Baxter Healthcare Corp - FDA 510(k) Cleared Devices
505
Total
496
Cleared
0
Denied
Baxter Healthcare Corp has 496 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 496 cleared submissions from 1977 to 2019.
Browse the FDA 510(k) cleared devices submitted by Baxter Healthcare Corp Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Baxter Healthcare Corp
505 devices
Cleared
Jul 25, 2019
PrisMax System Version 2
Gastroenterology & Urology
108d
Cleared
May 03, 2017
PrisMax Control Unit
Gastroenterology & Urology
138d
Cleared
Apr 08, 2014
ULTRAFUSE
Orthopedic
403d
Cleared
Oct 08, 2013
NEUTRAL LUER ACTIVATED DEVICE (ONE-LINK NEEDLE-FREE IV CONNECTOR) AND...
General Hospital
35d
Cleared
Mar 01, 2013
LARGE BORE STOPCOCK WITH ROTATING MALE LUER LOCK/LARGE BORE STOPCOCK WITH...
General Hospital
29d
Cleared
Jan 10, 2013
INTERLINK SYSTEM BURETROL SOLUTION SETS, INTERLINK SYSTEM BURETROL SOLUTION...
General Hospital
24d
Cleared
Jan 08, 2013
INTERLINK SYSTEM LEVER LOCK CANNULA WITH CHECK VALVE, SECONDARY MEDICATION...
General Hospital
22d
Cleared
Jun 29, 2012
FLOWEASE [SUBCUTANEOUS] INFUSION SET
General Hospital
80d
Cleared
Dec 08, 2011
NON-DEHP MICRO-VOLUME EXTENSION SET WITH 0.22 MICRON FILTER
General Hospital
37d
Cleared
Jun 14, 2011
ADDITIVE CAP
General Hospital
43d
Cleared
Mar 30, 2011
HOMECHOICE/HOMECHOICE PRO AUTOMATED PERSONAL CYCLER PERITONEAL DIALYSIS...
Gastroenterology & Urology
177d
Cleared
Mar 25, 2011
INTERLINK S / CLEARLINK SYSTEM / V-LINK LAD WITH VITALSHIELD PROTECTIVE...
General Hospital
113d
Looking for a specific device from Baxter Healthcare Corp? Search by device name or K-number.
Search all Baxter Healthcare Corp devices