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FDA 510(k)

KODAK KODAFLEX II CASSETTE

K-Number: K875083 · 1988-01-19

Decision Date1988-01-19
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK KODAFLEX II CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K875083. The device is classified under product code IXA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK KODAFLEX II CASSETTE?

KODAK KODAFLEX II CASSETTE is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Eastman Kodak Company. The 510(k) number is K875083.

When did KODAK KODAFLEX II CASSETTE receive FDA 510(k) clearance?

KODAK KODAFLEX II CASSETTE received FDA 510(k) clearance on 1988-01-19, under 510(k) number K875083.

Who is the listed applicant for KODAK KODAFLEX II CASSETTE?

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

What is the FDA product code for KODAK KODAFLEX II CASSETTE?

The FDA product code for KODAK KODAFLEX II CASSETTE is IXA.

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 Eastman Kodak Company 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.

View all 238 devices →

Related Devices (Code: IXA)

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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