Mps Acacia is one of 19031 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mps Acacia - FDA 510(k) Cleared Devices
Recent clearances: MPS ACACIA POWER INJECTABLE INFUSION SET, MPS ACACIA ENTERAL FEEDING TUBE, MPS ACACIA MEDFLO ELASTOMERIC PUMP
7
Total
7
Cleared
0
Denied
Mps Acacia has 7 FDA 510(k) cleared medical devices. Based in Brea, US.
Historical record: 7 cleared submissions from 2001 to 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Mps Acacia Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by California Department of Health Services and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Mps Acacia
7 devices
Cleared
Apr 28, 2009
MPS ACACIA POWER INJECTABLE INFUSION SET
General Hospital
34d
Cleared
May 14, 2008
MPS ACACIA ENTERAL FEEDING TUBE
Gastroenterology & Urology
97d
Cleared
Dec 08, 2005
MPS ACACIA MEDFLO ELASTOMERIC PUMP
General Hospital
92d
Cleared
Dec 08, 2005
MPS ACACIA NERVE BLOCK NEEDLE
Anesthesiology
49d
Cleared
Nov 13, 2003
MPS ACACIA SAFEGUARD HUBER DEVICE
General Hospital
52d
Cleared
Jul 09, 2001
MPS ACACIA MEDFLO INFUSION (LI) AND MPS ACACIA MEDFLO INFUSION (LI) KEEP VEIN...
General Hospital
88d
Cleared
Jan 12, 2001
MPS ACACIA PAIN KIT
General Hospital
64d