PERLINK CASSETTE, KIRAN CASSETTE
K-Number: K896708 · 1990-05-07
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Device Summary
Frequently Asked Questions
What is the PERLINK CASSETTE, KIRAN CASSETTE?
PERLINK CASSETTE, KIRAN CASSETTE is a medical device that received FDA 510(k) clearance on 1990-05-07. The listed applicant is Perlink USA, Inc.. The 510(k) number is K896708.
When did PERLINK CASSETTE, KIRAN CASSETTE receive FDA 510(k) clearance?
PERLINK CASSETTE, KIRAN CASSETTE received FDA 510(k) clearance on 1990-05-07, under 510(k) number K896708.
Who is the listed applicant for PERLINK CASSETTE, KIRAN CASSETTE?
The FDA 510(k) record lists Perlink USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERLINK CASSETTE, KIRAN CASSETTE?
The FDA product code for PERLINK CASSETTE, KIRAN 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 Perlink USA, 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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