POLAROID RADIOGRAPHIC FILM CASSETTE
K-Number: K812089 · 1981-08-31
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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