FDA 510(k)

MEDI VIEW

K-Number: K812152 · 1981-09-09

Decision Date1981-09-09

Product CodeIXC

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MEDI VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Medical Synergy. It received FDA 510(k) clearance on 1981-09-09 under 510(k) number K812152. The device is classified under product code IXC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI VIEW?

MEDI VIEW is a medical device that received FDA 510(k) clearance on 1981-09-09. The listed applicant is Medical Synergy. The 510(k) number is K812152.

When did MEDI VIEW receive FDA 510(k) clearance?

MEDI VIEW received FDA 510(k) clearance on 1981-09-09, under 510(k) number K812152.

Who is the listed applicant for MEDI VIEW?

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

What is the FDA product code for MEDI VIEW?

The FDA product code for MEDI VIEW is IXC.

Other records listing Medical Synergy 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.

K812735CLOTH SURGICAL GLOVES

Related Devices (Code: IXC)

K991302SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUSSmartlight, Inc.K973965SMART MOTORIZED VIEWERSmartlight, Ltd.K973115ARRIPRO 35 ST/TVArnold & Richter Cine Technik K970240DIFFUSER PANELFocused Viewer, Inc.K954998LILY DARK VIEWERLily Imaging Solutions Co.K954199VOXBOXVoxel

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.