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FDA 510(k)

DIGITAL MEDIA CONVERTER (D-MC)

K-Number: K935026 · 1994-08-24

ApplicantEigen Video
Decision Date1994-08-24
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL MEDIA CONVERTER (D-MC) is the device name listed in this FDA 510(k) record. The listed applicant is Eigen Video. It received FDA 510(k) clearance on 1994-08-24 under 510(k) number K935026. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL MEDIA CONVERTER (D-MC)?

DIGITAL MEDIA CONVERTER (D-MC) is a medical device that received FDA 510(k) clearance on 1994-08-24. The listed applicant is Eigen Video. The 510(k) number is K935026.

When did DIGITAL MEDIA CONVERTER (D-MC) receive FDA 510(k) clearance?

DIGITAL MEDIA CONVERTER (D-MC) received FDA 510(k) clearance on 1994-08-24, under 510(k) number K935026.

Who is the listed applicant for DIGITAL MEDIA CONVERTER (D-MC)?

The FDA 510(k) record lists Eigen Video as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL MEDIA CONVERTER (D-MC)?

The FDA product code for DIGITAL MEDIA CONVERTER (D-MC) is IZI.

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 Eigen Video 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.

K942264DDR WITH DPA AND 30/60 OPTIONS (DIGITAL VIEWSTATION)K850080DIGITAL IMAGE PROCESSOR FP-2CK844375EIGEN FLORO-STOR FS-100

Related Devices (Code: IZI)

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.

K261037780 nm SPY Portable Handheld Imaging (SPY-PHI) SystemStryker EndoscopyK253181SURGIMAGE SIM 1000H Fluorescence Imaging PlatformSurgimage CorporationK243645IC-Flow™ Imaging System 2.0Diagnostic Green GmbHK243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K231986Modus IRSynaptive Medical, Inc.K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision GmbH

Official Source

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

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