HEMORRHOIDAL LIGATION INSTR. SYSTEM— 510(k) K801352

Name: FDA 510(k) clearance K801352
Creator: U.S. Food and Drug Administration
Published: 1980-07-08

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K801352 for HEMORRHOIDAL LIGATION INSTR. SYSTEM, Substantially Equivalent on 1980-07-08. Applicant: Depuy, Inc.. Device class: 2.

Clearance details

Applicant: Depuy, Inc.
Product code: Code FHN
Device class: Class 2
Regulation: 21 CFR 876.4400
Advisory panel: Gastroenterology, Urology
Date received: 1980-06-09
Decision date: 1980-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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