JPI X-RAY FILM CASSETTE
K-Number: K930244 · 1993-04-07
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Device Summary
Frequently Asked Questions
What is the JPI X-RAY FILM CASSETTE?
JPI X-RAY FILM CASSETTE is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Jpi, Inc.. The 510(k) number is K930244.
When did JPI X-RAY FILM CASSETTE receive FDA 510(k) clearance?
JPI X-RAY FILM CASSETTE received FDA 510(k) clearance on 1993-04-07, under 510(k) number K930244.
Who is the listed applicant for JPI X-RAY FILM CASSETTE?
The FDA 510(k) record lists Jpi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JPI X-RAY FILM CASSETTE?
The FDA product code for JPI X-RAY FILM CASSETTE 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 Jpi, Inc. 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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