Penox Technologies, Inc.
Penox Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1987.
Top product codes for Penox Technologies, Inc.
Recent clearances by Penox Technologies, Inc.
- K864667 — PENOX HOSPITAL BED
- K863978 — PORTABLE LIQUID OXYGEN UNIT (MODIFICATION)
- K862654 — MODIFIED PENOX LIFT CHAIR
- K853775 — PENOX HIGH FLOW MANIFOLD
- K852109 — PENOX PERFORMER WHEELCHAIR
- K851218 — PENOX LIFT CHAIR
- K851215 — T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTER
- K851216 — PENOX DUAL FEED MANIFOLD
- K851217 — PENOX DUAL FLOW MINIFOLD
- K851219 — FILL HOSE SAFETY ADAPTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.