Martell Medical Products, Inc.
Walker, MI, US
Martell Medical Products, Inc. appears in FDA device records in Walker, MI. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Martell Medical Products, Inc. between 1981 and 1995. The busiest year on record is 1982, with 3. The most recent is 1995, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 1 |
| 1982 | 3 |
| 1984 | 1 |
| 1994 | 1 |
| 1995 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K945454 | LEUR TIP CAP, VLT CAP(TM) | JKA | Substantially Equivalent | |
| K944941 | PISTON SYRINGE | CBT | Substantially Equivalent | |
| K841810 | MARK5 ARTERIAL BLOOD GAS KIT | FMF | Substantially Equivalent | |
| K822786 | MDM ARTERIAL BLOOD GAS KIT | CBT | Substantially Equivalent | |
| K822760 | ARTERIAL LINE KIT | FMF | Substantially Equivalent | |
| K821096 | A-LINER | FMF | Substantially Equivalent | |
| K812560 | MDM ARTERIAL BLOOD GAS SYRINGE | FMF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain