ATRIUM'S HYBRID PTFE— 510(k) K933391

Unknown

Atrium Medical Corp.

FDA 510(k) clearance K933391 for ATRIUM'S HYBRID PTFE, Unknown on 1994-12-15. Applicant: Atrium Medical Corp.. Device class: 2.

Clearance details

Applicant: Atrium Medical Corp.
Product code: Code DYF
Device class: Class 2
Regulation: 21 CFR 870.3450
Advisory panel: Cardiovascular
Date received: 1993-07-12
Decision date: 1994-12-15
Decision: Unknown
Clearance type: Traditional
Location: Hollis, NH, 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.