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FDA 510(k)

X-RAY BEAM FILTER

K-Number: K837334 · 1983-04-22

ApplicantEastman Kodak Company
Decision Date1983-04-22
Product Code
DecisionSubstantially Equivalent

Device Summary

X-RAY BEAM FILTER 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 1983-04-22 under 510(k) number K837334. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY BEAM FILTER?

X-RAY BEAM FILTER is a medical device that received FDA 510(k) clearance on 1983-04-22. The listed applicant is Eastman Kodak Company. The 510(k) number is K837334.

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

X-RAY BEAM FILTER received FDA 510(k) clearance on 1983-04-22, under 510(k) number K837334.

Who is the listed applicant for X-RAY BEAM FILTER?

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

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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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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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