FDA 510(k)

CAT-A-KIT

K-Number: K760920 · 1976-11-09

Decision Date1976-11-09

Product CodeCHT

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

CAT-A-KIT is the device name listed in this FDA 510(k) record. The listed applicant is The Upjohn Co.. It received FDA 510(k) clearance on 1976-11-09 under 510(k) number K760920. The device is classified under product code CHT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAT-A-KIT?

CAT-A-KIT is a medical device that received FDA 510(k) clearance on 1976-11-09. The listed applicant is The Upjohn Co.. The 510(k) number is K760920.

When did CAT-A-KIT receive FDA 510(k) clearance?

CAT-A-KIT received FDA 510(k) clearance on 1976-11-09, under 510(k) number K760920.

Who is the listed applicant for CAT-A-KIT?

The FDA 510(k) record lists The Upjohn Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAT-A-KIT?

The FDA product code for CAT-A-KIT is CHT.

Other records listing The Upjohn 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.

K902004TROBICIN SUSCEPTIBILITY POWDER K900455ZEFAZONE SUSCEPTIBILITY POWDER K810853CK-TOTAL/CK-B (NAC) BIOLUMIN. ASSAY KIT K782009RIA KIT, PROGESTERONE K780792TESTOSTERONE RADIOIMMUNOASSAY KIT 125I

Related Devices (Code: CHT)

K913196KODAK EKTACHEM DT SLIDES (LIPASE)Eastman Kodak Company

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.