HEMOCLIP X-20 AUTOMATIC HEMOCLIP LIGATING APPLIER— 510(k) K844836

Name: FDA 510(k) clearance K844836
Creator: U.S. Food and Drug Administration
Published: 1985-01-23

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K844836 for HEMOCLIP X-20 AUTOMATIC HEMOCLIP LIGATING APPLIER, Substantially Equivalent on 1985-01-23. Applicant: Edward Weck, Inc.. Device class: 2.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code GWD
Device class: Class 2
Regulation: 21 CFR 866.3220
Advisory panel: Microbiology
Date received: 1984-12-12
Decision date: 1985-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Research Triangle Pa, NC, US

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