Penox Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K864667 | PENOX HOSPITAL BED | January 21, 1987 |
| K863978 | PORTABLE LIQUID OXYGEN UNIT (MODIFICATION) | December 15, 1986 |
| K862654 | MODIFIED PENOX LIFT CHAIR | July 18, 1986 |
| K853775 | PENOX HIGH FLOW MANIFOLD | November 29, 1985 |
| K852109 | PENOX PERFORMER WHEELCHAIR | August 22, 1985 |
| K851218 | PENOX LIFT CHAIR | June 21, 1985 |
| K851219 | FILL HOSE SAFETY ADAPTER | June 18, 1985 |
| K851217 | PENOX DUAL FLOW MINIFOLD | June 18, 1985 |
| K851216 | PENOX DUAL FEED MANIFOLD | June 18, 1985 |
| K851215 | T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTER | June 18, 1985 |