OP-CON SURG. INSTRUMENT #3— 510(k) K834171

Name: FDA 510(k) clearance K834171
Creator: U.S. Food and Drug Administration
Published: 1984-04-04

Substantially Equivalent

Imm Enterprises , Ltd.

FDA 510(k) clearance K834171 for OP-CON SURG. INSTRUMENT #3, Substantially Equivalent on 1984-04-04. Applicant: Imm Enterprises , Ltd.. Device class: 1.

Clearance details

Applicant: Imm Enterprises , Ltd.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1983-11-21
Decision date: 1984-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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