CATHETER CONNECTOR, ARGYLE TUBING— 510(k) K760524

Name: FDA 510(k) clearance K760524
Creator: U.S. Food and Drug Administration
Published: 1976-11-02

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K760524 for CATHETER CONNECTOR, ARGYLE TUBING, Substantially Equivalent on 1976-11-02. Applicant: Sherwood Medical Industries. Device class: 1.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code GCD
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1976-08-26
Decision date: 1976-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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