ST. MARK'S RECTAL BIOPSY FORCEPS— 510(k) K822401

Substantially Equivalent

Keymed, Inc.

FDA 510(k) clearance K822401 for ST. MARK'S RECTAL BIOPSY FORCEPS, Substantially Equivalent on 1982-08-27. Applicant: Keymed, Inc.. Device class: 1.

Clearance details

Applicant: Keymed, Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1982-08-10
Decision date: 1982-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.