CATHETER, ARGYLE THORACIC— 510(k) K760351

Name: FDA 510(k) clearance K760351
Creator: U.S. Food and Drug Administration
Published: 1976-08-23

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K760351 for CATHETER, ARGYLE THORACIC, Substantially Equivalent on 1976-08-23. Applicant: Sherwood Medical Industries. Device class: 1.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1976-08-02
Decision date: 1976-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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