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FDA 510(k) Applications Submitted by LAURA WORFOLK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K061803
06/27/2006
STA - CONTROL LA 1+2
DIAGNOSTICA STAGO, INC.
K061805
06/27/2006
STA - STACLOT DRVV SCREEN; STA - STACLOT DRVV CONFIRM
DIAGNOSTICA STAGO, INC.
K990046
01/07/1999
PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR VIII DEFICIENT PLASMA
PACIFIC HEMOSTASIS
K000679
02/29/2000
THROMBOSTRATE CONTROL PLASMAS
PACIFIC HEMOSTASIS
K971428
04/17/1997
COAGULATION CONTROL PLASMA(ABNORMAL)LEVEL 0
PACIFIC HEMOSTASIS
K992130
06/23/1999
PACIFIC HEMOSTASIS THROMBOSCREEN 400C
PACIFIC HEMOSTASIS
K992278
07/07/1999
HEPARIN CONTROL PLASMA LEVEL 1
PACIFIC HEMOSTASIS
K992279
07/07/1999
HEPARIN CONTROL PLASMA LEVEL 2
PACIFIC HEMOSTASIS
K972627
07/14/1997
PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR V DEFICIENT PLASMA (THROMBOSDREEN BRAND) (100056)
PACIFIC HEMOSTASIS
K994100
12/03/1999
PACIFIC HEMOSTASIS THROMBOPLASTIN D
PACIFIC HEMOSTASIS
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