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FDA 510(k)

DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE

K-Number: K828562 · 1983-04-28

ApplicantDigirad Corp.
Decision Date1983-04-28
Product Code
DecisionSubstantially Equivalent

Device Summary

DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Digirad Corp.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K828562. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE?

DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Digirad Corp.. The 510(k) number is K828562.

When did DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE receive FDA 510(k) clearance?

DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE received FDA 510(k) clearance on 1983-04-28, under 510(k) number K828562.

Who is the listed applicant for DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE?

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

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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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