THE INQUINAL RESORVOIR INSERTER— 510(k) K802983

Name: FDA 510(k) clearance K802983
Creator: U.S. Food and Drug Administration
Published: 1980-12-30

Substantially Equivalent

Lone Star Medical Products, Inc.

FDA 510(k) clearance K802983 for THE INQUINAL RESORVOIR INSERTER, Substantially Equivalent on 1980-12-30. Applicant: Lone Star Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Lone Star Medical Products, Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1980-11-21
Decision date: 1980-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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