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FDA 510(k)

KODAFLEX II RADIATION THERAPY L CASSETTE

K-Number: K885178 · 1989-02-03

ApplicantEastman Kodak Company
Decision Date1989-02-03
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAFLEX II RADIATION THERAPY L 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 1989-02-03 under 510(k) number K885178. 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 KODAFLEX II RADIATION THERAPY L CASSETTE?

KODAFLEX II RADIATION THERAPY L CASSETTE is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Eastman Kodak Company. The 510(k) number is K885178.

When did KODAFLEX II RADIATION THERAPY L CASSETTE receive FDA 510(k) clearance?

KODAFLEX II RADIATION THERAPY L CASSETTE received FDA 510(k) clearance on 1989-02-03, under 510(k) number K885178.

Who is the listed applicant for KODAFLEX II RADIATION THERAPY L 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 KODAFLEX II RADIATION THERAPY L CASSETTE?

The FDA product code for KODAFLEX II RADIATION THERAPY L CASSETTE 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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