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FDA 510(k)

KODAK T-MAT M FILM SO-245

K-Number: K860754 · 1986-03-06

ApplicantEastman Kodak Company
Decision Date1986-03-06
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK T-MAT M FILM SO-245 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 1986-03-06 under 510(k) number K860754. 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 T-MAT M FILM SO-245?

KODAK T-MAT M FILM SO-245 is a medical device that received FDA 510(k) clearance on 1986-03-06. The listed applicant is Eastman Kodak Company. The 510(k) number is K860754.

When did KODAK T-MAT M FILM SO-245 receive FDA 510(k) clearance?

KODAK T-MAT M FILM SO-245 received FDA 510(k) clearance on 1986-03-06, under 510(k) number K860754.

Who is the listed applicant for KODAK T-MAT M FILM SO-245?

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 M FILM SO-245?

The FDA product code for KODAK T-MAT M FILM SO-245 is IXA.

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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.

K060550KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386K060137KODAK ECLIPSE IMAGE PROCESSING SOFTWAREK060079KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEMK060055KODAK PACSK053347KODAK CARESTREAM PACSK051483KODAK DIRECTVIEW DR SYSTEM DETECTOR

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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.

K081557PORTABLE SUPINE PATIENT SUPPORT AND CASSETTE HOLDERJddb Manufacturing, Inc.K053173DS CASSETTEKonica Minolta Medical & Graphic, Inc.K040378KODAK DIRECTVIEW CR CASSETTE/GP/15 X 30 CM, CATALOG# 8418253Eastman Kodak CompanyK023020AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTEAgfa Corp.K021903KODAK X-OMAT CASSETTE/LEADLESS FOR DENTAL USEEastman Kodak CompanyK013686KODAK DIRECTVIEW TABLETOP CASSETTEEastman 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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