Medi USA, LP
FDA Regulatory Profile
Medi USA, LP 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 July 7, 2022.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K221654 | medi pneumatic compression system (pcs)-genius (Model 652) | July 7, 2022 |
| K183631 | medi pneumatic compression system (pcs) brio (Model 651) | January 25, 2019 |
| K051324 | MEDI BUTLER | December 5, 2005 |
| K941926 | MEDI STRUMPF | June 15, 1994 |