Company ยท US
Acacia Laboratories, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1995. Name variants (Inc, Corp, punctuation) are merged.
12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| KMF | Bandage, Liquid | 2 |
| LYV | Label Or Tag, Sterile | 2 |
| MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | 2 |
| BYY | Tube, Aspirating, Flexible, Connecting | 1 |
| DWS | Instruments, Surgical, Cardiovascular | 1 |
| FCM | Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) | 1 |
| KKX | Drape, Surgical, Antimicrobial | 1 |
| KNY | Accessories, Catheter, G-U | 1 |
| KRI | Accessory Equipment, Cardiopulmonary Bypass | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 26, 1995 | K952419 | STERIGAUZE GEL DRESSING Acacia Laboratories, Inc. | MGQ |
| Jul 12, 1995 | K952420 | STERIGAUZE WET DRESSING Acacia Laboratories, Inc. | KMF |
| Jul 11, 1995 | K951861 | STERICARE WOUND CARE GEL Acacia Laboratories, Inc. | MGQ |
| Jun 23, 1995 | K952414 | PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER Acacia Laboratories, Inc. | KNY |
| May 15, 1995 | K951914 | HYDRACARE ABSORBENT WOUND DRESSING Acacia Laboratories, Inc. | KMF |
| Mar 24, 1995 | K950344 | HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER Acacia Laboratories, Inc. | FCM |
| Mar 12, 1992 | K913408 | STERILE PLASTIC DRAPE Acacia Laboratories, Inc. | KKX |
| May 7, 1990 | K901761 | STERILE SUCTION TUBING SET Acacia Laboratories, Inc. | BYY |
| Nov 8, 1989 | K892856 | NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS Acacia Laboratories, Inc. | KRI |
| Jul 14, 1989 | K892804 | NEWCHILL(TM) CARDIAC INSULATOR Acacia Laboratories, Inc. | DWS |
| Oct 13, 1988 | K884055 | SURGI-TAG(TM) STERILE LABEL SETS Acacia Laboratories, Inc. | LYV |
| Oct 13, 1988 | K883654 | STERI-TAG(TM) STERILE LABEL SETS Acacia Laboratories, Inc. | LYV |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||