SUTURE REMOVAL SET CAT.#906— 510(k) K802019

Name: FDA 510(k) clearance K802019
Creator: U.S. Food and Drug Administration
Published: 1980-09-16

Substantially Equivalent

Pollak (Intl.), Ltd.

FDA 510(k) clearance K802019 for SUTURE REMOVAL SET CAT.#906, Substantially Equivalent on 1980-09-16. Applicant: Pollak (Intl.), Ltd.. Device class: 1.

Clearance details

Applicant: Pollak (Intl.), Ltd.
Product code: Code KDD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1980-08-20
Decision date: 1980-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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