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

FDA 510(k)

UNIVERSAL DIGITAL INTERFACE (UDI) 1717

K-Number: K103599 · 2011-04-27

ApplicantMeridian Medical Systems, LLC
Decision Date2011-04-27
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL DIGITAL INTERFACE (UDI) 1717 is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Medical Systems, LLC. It received FDA 510(k) clearance on 2011-04-27 under 510(k) number K103599. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL DIGITAL INTERFACE (UDI) 1717?

UNIVERSAL DIGITAL INTERFACE (UDI) 1717 is a medical device that received FDA 510(k) clearance on 2011-04-27. The listed applicant is Meridian Medical Systems, LLC. The 510(k) number is K103599.

When did UNIVERSAL DIGITAL INTERFACE (UDI) 1717 receive FDA 510(k) clearance?

UNIVERSAL DIGITAL INTERFACE (UDI) 1717 received FDA 510(k) clearance on 2011-04-27, under 510(k) number K103599.

Who is the listed applicant for UNIVERSAL DIGITAL INTERFACE (UDI) 1717?

The FDA 510(k) record lists Meridian Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL DIGITAL INTERFACE (UDI) 1717?

The FDA product code for UNIVERSAL DIGITAL INTERFACE (UDI) 1717 is MQB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Meridian Medical Systems, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K162687Paragon 2K112527UNIVERSAL DIGITAL INTERFACE (UDI) 1717K111305UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W

Related Devices (Code: MQB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, Inc.

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.

↑