HEIFETZ ANEURYSM CLIP, LMM BLADE— 510(k) K790413

Name: FDA 510(k) clearance K790413
Creator: U.S. Food and Drug Administration
Published: 1979-03-16

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K790413 for HEIFETZ ANEURYSM CLIP, LMM BLADE, Substantially Equivalent on 1979-03-16. Applicant: Edward Weck, Inc.. Device class: 2.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code HCH
Device class: Class 2
Regulation: 21 CFR 882.5200
Advisory panel: Neurology
Date received: 1979-02-26
Decision date: 1979-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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