Rmp Co.
FDA Regulatory Profile
Rmp Co. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 7, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K981844 | SLEEP MANAGEMENT SYSTEM | August 7, 1998 |
| K862197 | RMP COMPANT CRICOTHYROTOMY EQUIPMENT STORAGE TRAY | June 19, 1986 |
| K862154 | VENESECTION EQUIPMENT STORAGE TRAY | June 16, 1986 |
| K832697 | RMP INTUBATION EQUIP. STORAGE TRAY | December 27, 1983 |