ANCHOR BRAND SURGICAL NEEDLES— 510(k) K831648

Name: FDA 510(k) clearance K831648
Creator: U.S. Food and Drug Administration
Published: 1983-08-16

Substantially Equivalent

Anchor Products Co.

FDA 510(k) clearance K831648 for ANCHOR BRAND SURGICAL NEEDLES, Substantially Equivalent on 1983-08-16. Applicant: Anchor Products Co.. Device class: 1.

Clearance details

Applicant: Anchor Products Co.
Product code: Code GAB
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1983-05-23
Decision date: 1983-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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