FDA 510(k) Applications Submitted by MICHAEL D BICK, PH.D.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K960438 |
01/31/1996 |
TINTELIZE PAI-1 KIT |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K961724 |
05/03/1996 |
U-DOA CONTROLS |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K981752 |
05/18/1998 |
I-STAT COAGULATION CONTROL SET |
BIOPOOL INTL., INC. |
K972209 |
06/11/1997 |
SPECTROLYSE HEPARIN (ANTI-IIA) |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K962489 |
06/26/1996 |
CHROMOLIZE TPA ASSAY KIT |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K002642 |
08/24/2000 |
MINIQUANT D-DIMER, MODEL 1447 |
BIOPOOL INTL., INC. |
K983898 |
11/03/1998 |
BIOCLOT APC SENSITIVITY |
BIOPOOL INTL., INC. |
K955115 |
11/09/1995 |
VENOM TIEM REAGENT |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K955738 |
12/15/1995 |
BIOCLOT PROTEIN S |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K960871 |
03/04/1996 |
SPECTROLYSE ANTITHROMBIN III (ANTI-XA) |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K961370 |
04/09/1996 |
LA POSITIVE CONTROL PLASMA |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
K963106 |
08/12/1996 |
CHROMOLIZE PAI-1 KIT |
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC. |
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