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FDA 510(k)

POLAROID RADIOGRAPHIC FILM CASSETTE

K-Number: K812089 · 1981-08-31

Decision Date1981-08-31
Product Code
DecisionSubstantially Equivalent

Device Summary

POLAROID RADIOGRAPHIC FILM CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Polaroid Corp.. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K812089. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLAROID RADIOGRAPHIC FILM CASSETTE?

POLAROID RADIOGRAPHIC FILM CASSETTE is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Polaroid Corp.. The 510(k) number is K812089.

When did POLAROID RADIOGRAPHIC FILM CASSETTE receive FDA 510(k) clearance?

POLAROID RADIOGRAPHIC FILM CASSETTE received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812089.

Who is the listed applicant for POLAROID RADIOGRAPHIC FILM CASSETTE?

The FDA 510(k) record lists Polaroid Corp. 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.

Other records listing Polaroid Corp. 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.

Official Source

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