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FDA 510(k)

X-RAY CASSETTE

K-Number: K827379 · 1982-05-19

ApplicantSynchroplan Corp.
Decision Date1982-05-19
Product Code
DecisionSubstantially Equivalent

Device Summary

X-RAY CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Synchroplan Corp.. It received FDA 510(k) clearance on 1982-05-19 under 510(k) number K827379. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY CASSETTE?

X-RAY CASSETTE is a medical device that received FDA 510(k) clearance on 1982-05-19. The listed applicant is Synchroplan Corp.. The 510(k) number is K827379.

When did X-RAY CASSETTE receive FDA 510(k) clearance?

X-RAY CASSETTE received FDA 510(k) clearance on 1982-05-19, under 510(k) number K827379.

Who is the listed applicant for X-RAY CASSETTE?

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

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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.

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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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