DEKNATEL DISPOSABLE GOOSEN VASCULAR PNCH— 510(k) K820258

Name: FDA 510(k) clearance K820258
Creator: U.S. Food and Drug Administration
Published: 1982-03-02

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K820258 for DEKNATEL DISPOSABLE GOOSEN VASCULAR PNCH, Substantially Equivalent on 1982-03-02. 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: 1982-02-01
Decision date: 1982-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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