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FDA 510(k)

Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System

K-Number: K212704 · 2021-09-24

ApplicantPhilips Medical Systems
Decision Date2021-09-24
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System is a medical device manufactured by Philips Medical Systems. It received FDA 510(k) clearance on 2021-09-24 under approval number K212704. 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 Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System?

Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2021-09-24. It is manufactured by Philips Medical Systems. The 510(k) number is K212704.

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

Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System received FDA 510(k) clearance on 2021-09-24, under approval number K212704.

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

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

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

The FDA product code for Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti 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 NCT05857852 Low-Intensity Focused Ultrasound for Cocaine Use Disorder COMPLETED NCT04981223 Predicting Location and Extent of Prostate Cancer Using Micro-Ultrasound Imaging COMPLETED NCT07608614 Sleep and Performance RECRUITING

Related PubMed Literature

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: 39943397 Clinical Validation of a Video-Otoscopy-Based Medical Device for the Remote Diagnosis of Ear Complaints. Sensors (Basel, Switzerland) (2025) PMID: 39892748 Long-term Safety and Performance of a Suprachoroidal Pressure Sensor System: Results of the EYEMATE-SC Trial Follow-up Study. Ophthalmology (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

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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.

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