Acacia Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acacia Laboratories, Inc. - FDA 510(k) Cleared Devices
12
Total
10
Cleared
0
Denied
Acacia Laboratories, Inc. has 10 FDA 510(k) cleared medical devices. Based in Santa Ana, US.
Historical record: 10 cleared submissions from 1988 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Acacia Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Acacia Laboratories, Inc.
12 devices
Cleared
Jul 26, 1995
STERIGAUZE GEL DRESSING
General & Plastic Surgery
64d
Cleared
Jul 12, 1995
STERIGAUZE WET DRESSING
General & Plastic Surgery
50d
Cleared
Jul 11, 1995
STERICARE WOUND CARE GEL
General & Plastic Surgery
81d
Cleared
Jun 23, 1995
PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER
Gastroenterology & Urology
31d
Cleared
May 15, 1995
HYDRACARE ABSORBENT WOUND DRESSING
General & Plastic Surgery
21d
Cleared
Mar 24, 1995
HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER
Gastroenterology & Urology
56d
Cleared
Mar 12, 1992
STERILE PLASTIC DRAPE
General Hospital
226d
Cleared
May 07, 1990
STERILE SUCTION TUBING SET
General Hospital
19d
Cleared
Nov 08, 1989
NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS
Cardiovascular
204d
Cleared
Jul 14, 1989
NEWCHILL(TM) CARDIAC INSULATOR
Cardiovascular
88d
Cleared
Oct 13, 1988
STERI-TAG(TM) STERILE LABEL SETS
General & Plastic Surgery
48d
Cleared
Oct 13, 1988
SURGI-TAG(TM) STERILE LABEL SETS
General & Plastic Surgery
17d