PENOX DUAL FLOW MINIFOLD— 510(k) K851217

Substantially Equivalent

Penox Technologies, Inc.

FDA 510(k) clearance K851217 for PENOX DUAL FLOW MINIFOLD, Substantially Equivalent on 1985-06-18. Applicant: Penox Technologies, Inc..

Clearance details

Applicant: Penox Technologies, Inc.
Product code: Code CAM
Advisory panel: Anesthesiology
Date received: 1985-03-26
Decision date: 1985-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittston, PA, US

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