L-F/KODAK FLEXIBLE GRID CASSETTE
K-Number: K883312 · 1988-08-16
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Device Summary
Frequently Asked Questions
What is the L-F/KODAK FLEXIBLE GRID CASSETTE?
L-F/KODAK FLEXIBLE GRID CASSETTE is a medical device that received FDA 510(k) clearance on 1988-08-16. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K883312.
When did L-F/KODAK FLEXIBLE GRID CASSETTE receive FDA 510(k) clearance?
L-F/KODAK FLEXIBLE GRID CASSETTE received FDA 510(k) clearance on 1988-08-16, under 510(k) number K883312.
Who is the listed applicant for L-F/KODAK FLEXIBLE GRID CASSETTE?
The FDA 510(k) record lists Mallinckrodt Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for L-F/KODAK FLEXIBLE GRID CASSETTE?
The FDA product code for L-F/KODAK FLEXIBLE GRID 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 Mallinckrodt Group, 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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