Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System

K-Number: K211597 · 2021-09-08

ApplicantPhilips Medical Systems
Decision Date2021-09-08
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System is a medical device manufactured by Philips Medical Systems. It received FDA 510(k) clearance on 2021-09-08 under approval number K211597. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System?

EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2021-09-08. It is manufactured by Philips Medical Systems. The 510(k) number is K211597.

When was EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System approved by the FDA?

EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System received FDA 510(k) clearance on 2021-09-08, under approval number K211597.

What company makes EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System?

EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System is manufactured by Philips Medical Systems.

What is the FDA product code for EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System?

The FDA product code for EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System is IYN.

Related Clinical Trials

NCT07040696 Accuracy of Venous Excess Ultrasound Score at Hospital Admission to Predict Acute Kidney Injury COMPLETED NCT01143454 Characterization of Patients With Uncommon Presentations and/or Uncommon Diseases Associated With the Cardiovascular System RECRUITING NCT07613476 Pregabalin Phonophoresis for Carpal Tunnel Syndrome Pain ACTIVE_NOT_RECRUITING NCT06642935 A Study to Explore Improved Features and a Simplified Treatment Approach for a Totally Implantable Cochlear Implant (TICI) Research System in Adults With Severe Hearing Loss ACTIVE_NOT_RECRUITING NCT05857852 Low-Intensity Focused Ultrasound for Cocaine Use Disorder COMPLETED NCT04981223 Predicting Location and Extent of Prostate Cancer Using Micro-Ultrasound Imaging COMPLETED

Related PubMed Literature

PMID: 42201559 Time-series and thematic analyses of clinical utilities and operational issues in early clinical studies of the da Vinci surgical system. Journal of robotic surgery (2026) PMID: 41887630 Capacity building for ethical use of artificial intelligence in health: protocol for a scoping review of training initiatives and gaps in Africa. BMJ open (2026) PMID: 41251011 Effectivity of the Dehydrated Human Amnion/Chorion Membrane Allograft for Diabetic Foot Ulcers in Japan: A Case Series. International wound journal (2025) PMID: 39943397 Clinical Validation of a Video-Otoscopy-Based Medical Device for the Remote Diagnosis of Ear Complaints. Sensors (Basel, Switzerland) (2025)

Other Devices by Philips Medical Systems

K161164CareEvent inclusive of the CareEvent Mobile Application accessory K153702M3290B Philips IntelliVue Information Center iX K160951Philips Efficia CMS200 Central Monitoring System K151812PATIENT MONITORS VARIOUS MODELS K172226MX40 Release B.07 K163584M3290B Philips IntelliVue Information Center iX

View all 15 devices →

Related Devices (Code: IYN)

K162845DC-40/DC-35/DC-45/DC-40S/DC-40 Pro Diagnostic Ultrasound SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. K162902ARIETTA Prologue Diagnostic Ultrasound system and TransducersHitachi , Ltd. K163138Clarius Ultrasound SystemClarius Mobile Health Corp. K163077LOGIQ E9, LOGIQ E9 XDClear 2.0GE Medical Systems Ultrasound and Primary Care Diagnostics K162583ALOKA LISENDO 880Hitachi , Ltd. K163020Xperius Ultrasound SystemPhilips Health Care

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑