Akcess Medical Products, Inc.
FDA 510(k) & PMA Approved Devices — 36 products
Advertisement
Total Devices36
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K926374 | SILICONE CATHETER REPAIR KITS | KOC | 1994-10-07 | View |
| 510(k) | K925819 | AKCESS0CATH KIT | LFJ | 1994-08-02 | View |
| 510(k) | K925818 | AKCESS-CATH | LFJ | 1994-04-05 | View |
| 510(k) | K930630 | RIGHT ATRIAL CATHETER | LJS | 1994-02-07 | View |
| 510(k) | K920634 | SPLITTABLE SHEATH INTRODUCER SET | LFJ | 1994-01-14 | View |
| 510(k) | K931120 | COAXIAL ACUTE CATHETER | LFJ | 1994-01-14 | View |
| 510(k) | K914936 | CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET | LFK | 1992-04-23 | View |
| 510(k) | K920331 | RIGHT ATRIAL CATHETER KITS | DQY | 1992-04-22 | View |
| 510(k) | K914826 | AKCESS-CATH KIT | LFJ | 1992-04-10 | View |
| 510(k) | K915215 | CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS | LFK | 1992-03-27 | View |
| 510(k) | K911333 | RIGHT ATRIAL CATHETERS | DQY | 1991-09-23 | View |
| 510(k) | K910502 | VESSEL DILATORS | FKA | 1991-04-29 | View |
| 510(k) | K910501 | PERMANENT SILICONE CATHETERS | LFJ | 1991-04-29 | View |
| 510(k) | K910572 | INJECTION CAPS | FOZ | 1991-04-29 | View |
| 510(k) | K910641 | INTRODUCER NEEDLES | KOC | 1991-04-29 | View |
| 510(k) | K910321 | Y ADAPTOR | KOC | 1991-04-16 | View |
| 510(k) | K904139 | SINGLE LUMEN CATHETER KITS | LFJ | 1990-12-04 | View |
| 510(k) | K904140 | SINGLE LUMEN CATHETERS, MODIFICATION | LFJ | 1990-11-27 | View |
| 510(k) | K904433 | DUAL LUMEN NEEDLES | LBW | 1990-11-23 | View |
| 510(k) | K902203 | TENCKHOFF PERITONEAL DIALYSIS KIT | FJG | 1990-08-01 | View |
No matching devices.
Advertisement