Pacific Hemostasis is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pacific Hemostasis - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Pacific Hemostasis has 29 FDA 510(k) cleared hematology devices. Based in Mchenry, US.
Historical record: 29 cleared submissions from 1978 to 2000.
Browse the complete list of FDA 510(k) cleared hematology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pacific Hemostasis
29 devices
Cleared
Mar 24, 2000
THROMBOSTRATE CONTROL PLASMAS
Hematology
24d
Cleared
Feb 18, 2000
PACIFIC HEMOSTASIS THROMBOPLASTIN D
Hematology
77d
Cleared
Sep 03, 1999
PACIFIC HEMOSTASIS THROMBOSCREEN 400C
Hematology
72d
Cleared
Aug 26, 1999
HEPARIN CONTROL PLASMA LEVEL 1
Hematology
50d
Cleared
Aug 26, 1999
HEPARIN CONTROL PLASMA LEVEL 2
Hematology
50d
Cleared
Jun 21, 1999
PACIFIC HEMOSTASIS THROMBOSCREEN 200
Hematology
63d
Cleared
Feb 17, 1999
PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR VIII DEFICIENT PLASMA
Hematology
41d
Cleared
Dec 01, 1998
COAGULATION CONTROL LEVEL 1 (NORMAL)
Hematology
13d
Cleared
Dec 01, 1998
COAGULATION CONTROL LEVEL 2 (ABNORMAL)
Hematology
13d
Cleared
Dec 01, 1998
COAGULATION CONTROL LEVEL 3 (ABNORMAL)
Hematology
13d
Cleared
Aug 13, 1997
PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR V DEFICIENT PLASMA (THROMBOSDREEN...
Hematology
30d
Cleared
Jun 17, 1997
COAGULATION CONTROL PLASMA(ABNORMAL)LEVEL 0
Hematology
61d