VACVENT— 510(k) K931873

Unknown

Steven Frank Mercereau

FDA 510(k) clearance K931873 for VACVENT, Unknown on 1993-12-30. Applicant: Steven Frank Mercereau. Device class: 1.

Clearance details

Applicant: Steven Frank Mercereau
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1993-04-14
Decision date: 1993-12-30
Decision: Unknown
Clearance type: Traditional
Location: Conyers, GA, 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.