Mar-Med Co
FDA Regulatory Profile
Mar-Med Co appears in FDA public data with 1 recall, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0945-2021, Class II) was initiated on December 28, 2020. Its most recent 510(k) clearance was granted on March 18, 1993.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-0945-2021 | Class II | Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Us | December 28, 2020 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K924223 | MAR-MED LIVER STRAP | March 18, 1993 |