AORTIC OCCLUDER #000390— 510(k) K792088

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K792088 for AORTIC OCCLUDER #000390, Substantially Equivalent on 1979-10-26. 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: 1979-10-17
Decision date: 1979-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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