Acacia, Inc. is one of 10912 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acacia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Extension Set with BD Q-Syte Luer Access Split Septum, ENTERAL NUTRITION WARMER, MEDI-SIS SYRINGE INFUSION SYSTEM
17
Total
17
Cleared
0
Denied
Acacia, Inc. has 17 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.
Historical record: 17 cleared submissions from 1979 to 2014.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Acacia, Inc.
17 devices
Cleared
Sep 19, 2014
Extension Set with BD Q-Syte Luer Access Split Septum
General Hospital
11d
Cleared
Jun 13, 2013
ENTERAL NUTRITION WARMER
General Hospital
304d
Cleared
Jan 13, 2012
MEDI-SIS SYRINGE INFUSION SYSTEM
General Hospital
241d
Cleared
Nov 10, 2010
BLOOD SAMPLING SET
General Hospital
14d
Cleared
Oct 27, 2009
ACACIA PISTON SYRINGE
General Hospital
29d
Cleared
Jul 15, 1998
FLOW-EZE BLUNT CANNULA (1999BC)
General Hospital
372d
Cleared
Sep 16, 1993
SPRING LOADED SYRINGE
General Hospital
197d
Cleared
Feb 14, 1992
ACACIAS PHARM/PUMP
General Hospital
235d
Cleared
Jul 06, 1990
LUER LOCK TRANSFER PIN
General Hospital
121d
Cleared
Mar 23, 1990
PHARMULATOR
General Hospital
100d
Cleared
Oct 27, 1989
INTOPO
General Hospital
130d
Cleared
Sep 12, 1989
SYRINGE TIP ADAPTOR
General Hospital
85d