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FDA 510(k)

VIDIVIEWER MOTORIZED MASS FILM VIEWER

K-Number: K828566 · 1983-01-03

Decision Date1983-01-03
Product Code
DecisionSubstantially Equivalent

Device Summary

VIDIVIEWER MOTORIZED MASS FILM VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Diversied P.A.. It received FDA 510(k) clearance on 1983-01-03 under 510(k) number K828566. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDIVIEWER MOTORIZED MASS FILM VIEWER?

VIDIVIEWER MOTORIZED MASS FILM VIEWER is a medical device that received FDA 510(k) clearance on 1983-01-03. The listed applicant is Diversied P.A.. The 510(k) number is K828566.

When did VIDIVIEWER MOTORIZED MASS FILM VIEWER receive FDA 510(k) clearance?

VIDIVIEWER MOTORIZED MASS FILM VIEWER received FDA 510(k) clearance on 1983-01-03, under 510(k) number K828566.

Who is the listed applicant for VIDIVIEWER MOTORIZED MASS FILM VIEWER?

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

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.

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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