DEKNATEL GOOSEN VASCULAR PUNCH BLADES— 510(k) K802079

Name: FDA 510(k) clearance K802079
Creator: U.S. Food and Drug Administration
Published: 1980-09-16

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K802079 for DEKNATEL GOOSEN VASCULAR PUNCH BLADES, Substantially Equivalent on 1980-09-16. Applicant: Howmedica Corp.. Device class: 1.

Clearance details

Applicant: Howmedica Corp.
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1980-08-28
Decision date: 1980-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.