Martech Medical Products
Martech Medical Products appears in FDA public data with 0 recalls, 11 510(k) clearances, 5 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on September 18, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 5
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K254095 | 25G Huber Needle | September 18, 2026 |
| K130855 | PTFE SUPER SHEATH INTRODUCER | July 29, 2013 |
| K120617 | PTFE SUPER SHEATH INTRODUCER | November 19, 2012 |
| K101399 | COAXIAL INTRODUCER SET | June 17, 2010 |
| K960519 | MARTECH ENDOSCOPIC INJECTION NEEDLE | May 1, 1996 |
| K931924 | MARKSMAN ARTERIAL BLOOD GAS SYRINGE | August 3, 1993 |
| K922438 | PRO2 OXYGEN ANALYZER | March 5, 1993 |
| K926007 | ACCESSORY TO PISTON SYRINGE | February 23, 1993 |
| K914778 | NEOLINE(TM) | September 16, 1992 |
| K910970 | MARKSMAN ARTERIAL BLOOD GAS SYRINGE | October 15, 1991 |
| K890473 | NEEDLE GUARD(TM) | April 3, 1989 |