PENOX DUAL FEED MANIFOLD— 510(k) K851216
Substantially EquivalentPenox Technologies, Inc.
FDA 510(k) clearance K851216 for PENOX DUAL FEED MANIFOLD, 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pittston, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.