Baxa Corp. is one of 21641 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baxa Corp. - FDA 510(k) Cleared Devices
Recent clearances: SURECONNECT CLOSED DRUG RECONSTITUTION AND TRANSFER SYSTEM, SWABBABLE CAP, MODEL 60205, REPEATER PUMP II TUBE SETS
8
Total
8
Cleared
0
Denied
Baxa Corp. has 8 FDA 510(k) cleared medical devices. Based in Englewood, US.
Historical record: 8 cleared submissions from 1994 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Baxa Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Baxa Corp.
8 devices
Cleared
Feb 19, 2010
SURECONNECT CLOSED DRUG RECONSTITUTION AND TRANSFER SYSTEM
General Hospital
324d
Cleared
Aug 03, 2007
SWABBABLE CAP, MODEL 60205
General Hospital
198d
Cleared
Mar 09, 2007
REPEATER PUMP II TUBE SETS
General Hospital
163d
Cleared
Aug 12, 2002
RAPID-FILL TUBESET, MODEL 90005
General Hospital
13d
Cleared
Mar 28, 2001
EXACTA-MIX 2400 COMPOUNDING SYSTEM, MODEL EXACTA-MIX 2400
General Hospital
210d
Cleared
Oct 06, 1998
MICROFUSE DUAL RATE INFUSER
General Hospital
14d
Cleared
Jun 21, 1995
PISTON SYRINGE
General Hospital
61d
Cleared
Feb 25, 1994
SYRINGE INFUSER
General Hospital
220d