X-RAY FILM CASSETTE
K-Number: K945858 · 1995-03-21
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Device Summary
Frequently Asked Questions
What is the X-RAY FILM CASSETTE?
X-RAY FILM CASSETTE is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is J.P.I. Chicago Co.. The 510(k) number is K945858.
When did X-RAY FILM CASSETTE receive FDA 510(k) clearance?
X-RAY FILM CASSETTE received FDA 510(k) clearance on 1995-03-21, under 510(k) number K945858.
Who is the listed applicant for X-RAY FILM CASSETTE?
The FDA 510(k) record lists J.P.I. Chicago Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-RAY FILM CASSETTE?
The FDA product code for 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 J.P.I. Chicago 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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