Company ยท US
Cd Medical, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1994. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| FKP | System, Dialysate Delivery, Single Patient | 3 |
| KOC | Accessories, Blood Circuit, Hemodialysis | 2 |
| FIF | Set, Dialysis, Single Needle With Uni-Directional Pump | 1 |
| FIP | Subsystem, Water Purification | 1 |
| FJK | Set, Tubing, Blood, With And Without Anti-Regurgitation Valve | 1 |
| FKQ | System, Dialysate Delivery, Central Multiple Patient | 1 |
| GBZ | Catheter, Cholangiography | 1 |
| KDI | Dialyzer, High Permeability With Or Without Sealed Dialysate System | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 30, 1994 | K925654 | CD HOME DIALYSERVICE HEMODIALYSIS TRAY Cd Medical, Inc. | KOC |
| Apr 9, 1991 | K910215 | DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYST Cd Medical, Inc. | FKP |
| Jun 26, 1990 | K901520 | WURTZ CHOLEY CLIP (TM) Cd Medical, Inc. | GBZ |
| Nov 8, 1989 | K894106 | DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST Cd Medical, Inc. | FIP |
| Dec 8, 1988 | K884353 | ULTRX(TM) 850 ARTIFICIAL KIDNEY Cd Medical, Inc. | KDI |
| Apr 13, 1988 | K880459 | 480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE Cd Medical, Inc. | FKP |
| Oct 23, 1987 | K873279 | 8810 PUMP-PUMP SINGLE NEEDLE DEVICE Cd Medical, Inc. | FIF |
| Jan 20, 1987 | K864784 | SERAFLO(TM) BLOODLINES FOR HEMODIALYSIS Cd Medical, Inc. | FJK |
| Sep 9, 1986 | K862304 | DRAKE WILLOCK CENTRAL DIALYSATE DELIVERY SYSTEM Cd Medical, Inc. | FKQ |
| Nov 6, 1985 | K853513 | DRAKE WILLOCK 480 UF CONTROL IDALYSATE DELIVERY SY Cd Medical, Inc. | FKP |
| Jan 3, 1985 | K844185 | MODIFIED C-DAK Cd Medical, Inc. | KOC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||