Pharmaseal Div., Baxter Healthcare Corp. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Pharmaseal Div., Baxter Healthcare Corp. has 24 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1976 to 1979.
Browse the FDA 510(k) cleared devices submitted by Pharmaseal Div., Baxter Healthcare Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Pharmaseal Div., Baxter Healthcare Corp.
24 devices
Cleared
Dec 10, 1979
HYPERALIMENTATION DRESSING TRAY
General Hospital
77d
Cleared
Dec 05, 1979
CONTINUOUS FLUSH DEVICE
Cardiovascular
44d
Cleared
Nov 05, 1979
PHADECODE XA INHIBITOR ASSAY
Hematology
27d
Cleared
Oct 22, 1979
VENTILATOR TUBE WITH FILTER
General Hospital
42d
Cleared
Jul 30, 1979
AMIPAQUE MYELOGRAM TRAY
General Hospital
39d
Cleared
Jun 05, 1979
TWO-WAY ANESTHESIA FILTER
General Hospital
28d
Cleared
Apr 24, 1979
LOW DEAD SPACE INSULIN SYRINGE
General Hospital
57d
Cleared
Jan 04, 1979
TRAY, AUXILLARY BLOCK
Anesthesiology
22d
Cleared
Nov 08, 1978
PREP TRAY, PREOPERATIVE SKIN
General & Plastic Surgery
16d
Cleared
Oct 06, 1978
MONITORING, PRESSURE KIT
Cardiovascular
4d
Cleared
Jun 22, 1978
IMPROVED DISPOSABLE HYPODERMIC NEEDLE
General & Plastic Surgery
27d
Cleared
Nov 17, 1977
PRESSURE TUBING
Cardiovascular
51d