VEIN-TRAP TM— 510(k) K811910

Substantially Equivalent

Atrium Medical Corp.

FDA 510(k) clearance K811910 for VEIN-TRAP TM, Substantially Equivalent on 1981-07-20. Applicant: Atrium Medical Corp.. Device class: 2.

Clearance details

Applicant: Atrium Medical Corp.
Product code: Code DWQ
Device class: Class 2
Regulation: 21 CFR 870.4885
Advisory panel: Cardiovascular
Date received: 1981-07-01
Decision date: 1981-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.