CASSETTE, RADIOGRAPHIC FILM
K-Number: K930220 · 1993-04-13
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Device Summary
Frequently Asked Questions
What is the CASSETTE, RADIOGRAPHIC FILM?
CASSETTE, RADIOGRAPHIC FILM is a medical device that received FDA 510(k) clearance on 1993-04-13. The listed applicant is X-Ray Accessories Mfg. Co.. The 510(k) number is K930220.
When did CASSETTE, RADIOGRAPHIC FILM receive FDA 510(k) clearance?
CASSETTE, RADIOGRAPHIC FILM received FDA 510(k) clearance on 1993-04-13, under 510(k) number K930220.
Who is the listed applicant for CASSETTE, RADIOGRAPHIC FILM?
The FDA 510(k) record lists X-Ray Accessories Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CASSETTE, RADIOGRAPHIC FILM?
The FDA product code for CASSETTE, RADIOGRAPHIC FILM 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 X-Ray Accessories Mfg. Co. 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.
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
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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