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FDA 510(k)

KODAK T-MAT C FILM SO-119

K-Number: K843149 · 1984-08-27

ApplicantEastman Kodak Company
Decision Date1984-08-27
Product CodeLWZ
DecisionSubstantially Equivalent

Device Summary

KODAK T-MAT C FILM SO-119 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 1984-08-27 under 510(k) number K843149. The device is classified under product code LWZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK T-MAT C FILM SO-119?

KODAK T-MAT C FILM SO-119 is a medical device that received FDA 510(k) clearance on 1984-08-27. The listed applicant is Eastman Kodak Company. The 510(k) number is K843149.

When did KODAK T-MAT C FILM SO-119 receive FDA 510(k) clearance?

KODAK T-MAT C FILM SO-119 received FDA 510(k) clearance on 1984-08-27, under 510(k) number K843149.

Who is the listed applicant for KODAK T-MAT C FILM SO-119?

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 T-MAT C FILM SO-119?

The FDA product code for KODAK T-MAT C FILM SO-119 is LWZ.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: LWZ)

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.

K843148KODAK T-MAT H FILM SO-118Eastman Kodak Company

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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