FDA 510(k) Applications Submitted by LAURA A 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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