Martell Medical Products, Inc.
Martell Medical Products, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 14, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K945454 | LEUR TIP CAP, VLT CAP(TM) | April 14, 1995 |
| K944941 | PISTON SYRINGE | December 5, 1994 |
| K841810 | MARK5 ARTERIAL BLOOD GAS KIT | July 6, 1984 |
| K822786 | MDM ARTERIAL BLOOD GAS KIT | October 21, 1982 |
| K822760 | ARTERIAL LINE KIT | September 28, 1982 |
| K821096 | A-LINER | May 14, 1982 |
| K812560 | MDM ARTERIAL BLOOD GAS SYRINGE | October 9, 1981 |