Company ยท US
Martech Medical Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2026. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| DYB | Introducer, Catheter | 3 |
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection | 2 |
| CBT | Arterial Blood Sampling Kit | 1 |
| CCL | Analyzer, Gas, Oxygen, Gaseous-Phase | 1 |
| FBK | Endoscopic Injection Needle, Gastroenterology-Urology | 1 |
| FMF | Syringe, Piston | 1 |
| FMI | Needle, Hypodermic, Single Lumen | 1 |
| PTI | Non-Coring (Huber) Needle | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 18, 2026 | K254095 | 25G Huber Needle Martech Medical Products | PTI |
| Jul 29, 2013 | K130855 | PTFE SUPER SHEATH INTRODUCER Martech Medical Products | DYB |
| Nov 19, 2012 | K120617 | PTFE SUPER SHEATH INTRODUCER Martech Medical Products | DYB |
| Jun 17, 2010 | K101399 | COAXIAL INTRODUCER SET Martech Medical Products | DYB |
| May 1, 1996 | K960519 | MARTECH ENDOSCOPIC INJECTION NEEDLE Martech Medical Products, Inc. | FBK |
| Aug 3, 1993 | K931924 | MARKSMAN ARTERIAL BLOOD GAS SYRINGE Martech Medical Products, Inc. | JKA |
| Mar 5, 1993 | K922438 | PRO2 OXYGEN ANALYZER Martech Medical Products, Inc. | CCL |
| Feb 23, 1993 | K926007 | ACCESSORY TO PISTON SYRINGE Martech Medical Products, Inc. | FMF |
| Sep 16, 1992 | K914778 | NEOLINE(TM) Martech Medical Products, Inc. | CBT |
| Oct 15, 1991 | K910970 | MARKSMAN ARTERIAL BLOOD GAS SYRINGE Martech Medical Products, Inc. | JKA |
| Apr 3, 1989 | K890473 | NEEDLE GUARD(TM) Martech Medical Products, Inc. | FMI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||