ACCU-VENT(TM) WITH NEEDLE-PRO(TM)— 510(k) K912043

Unknown

Concord/Portex

FDA 510(k) clearance K912043 for ACCU-VENT(TM) WITH NEEDLE-PRO(TM), Unknown on 1991-07-05. Applicant: Concord/Portex.

Clearance details

Applicant: Concord/Portex
Product code: Code CBT
Advisory panel: Anesthesiology
Date received: 1991-05-08
Decision date: 1991-07-05
Decision: Unknown
Clearance type: Traditional
Location: Keene, NH, US

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