Akcess Medical Products, Inc.
Akcess Medical Products, Inc. appears in FDA public data with 0 recalls, 36 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Oct 7, 1994.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 36
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K926374 | SILICONE CATHETER REPAIR KITS | Oct 7, 1994 |
| K925819 | AKCESS0CATH KIT | Aug 2, 1994 |
| K925818 | AKCESS-CATH | Apr 5, 1994 |
| K930630 | RIGHT ATRIAL CATHETER | Feb 7, 1994 |
| K920634 | SPLITTABLE SHEATH INTRODUCER SET | Jan 14, 1994 |
| K931120 | COAXIAL ACUTE CATHETER | Jan 14, 1994 |
| K914936 | CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET | Apr 23, 1992 |
| K920331 | RIGHT ATRIAL CATHETER KITS | Apr 22, 1992 |
| K914826 | AKCESS-CATH KIT | Apr 10, 1992 |
| K915215 | CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS | Mar 27, 1992 |
| K911333 | RIGHT ATRIAL CATHETERS | Sep 23, 1991 |
| K910501 | PERMANENT SILICONE CATHETERS | Apr 29, 1991 |
| K910572 | INJECTION CAPS | Apr 29, 1991 |
| K910502 | VESSEL DILATORS | Apr 29, 1991 |
| K910641 | INTRODUCER NEEDLES | Apr 29, 1991 |
| K910321 | Y ADAPTOR | Apr 16, 1991 |
| K904139 | SINGLE LUMEN CATHETER KITS | Dec 4, 1990 |
| K904140 | SINGLE LUMEN CATHETERS, MODIFICATION | Nov 27, 1990 |
| K904433 | DUAL LUMEN NEEDLES | Nov 23, 1990 |
| K902203 | TENCKHOFF PERITONEAL DIALYSIS KIT | Aug 1, 1990 |