CARDIOVASCULAR INSTRUMENTS-VARIOUS— 510(k) K791710

Name: FDA 510(k) clearance K791710
Creator: U.S. Food and Drug Administration
Published: 1979-09-12

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K791710 for CARDIOVASCULAR INSTRUMENTS-VARIOUS, Substantially Equivalent on 1979-09-12. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1979-08-27
Decision date: 1979-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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