FDA 510(k) Applications Submitted by JAMES F GODFREY
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K010030 |
01/03/2001 |
LIQUISPX HDL/LDL LIQUID CHOLESTEROL CALIBRATOR |
SYNERGENT BIOCHEM INC.-CLINICAL CONTROLS DIV. |
| K962432 |
06/24/1996 |
LIQUISPEX URINE (MICRO)ALBUMIN CONTROL |
CLINICAL CONTROLS, INC. |
| K012855 |
08/24/2001 |
LIQUISPX LIQUID LIPID CONTROL |
CLINICAL CONTROLS DIVISION |
| K012907 |
08/29/2001 |
LIQUISPX LIQUID SALIVA OR UNRINE DRUG OF ABUSE CONTROL |
CLINICAL CONTROLS |
| K964278 |
10/28/1996 |
WHOLE BLOOD GLUCOSE CONTROL LEVEL 1,2,AND 3/WHOLE BLOOD GLUCOSE LINEARITY CONTROL-LEVEL1,2,3,4,5,AND 6 |
CLINICAL CONTROLS, INC. |
| K955690 |
12/14/1995 |
AQUEOUS ETHANOL/AMMONIA CONTROL LEVEL 1, 2, & 3 |
CLINICAL CONTROLS, INC. |
| K955691 |
12/14/1995 |
SERUM VOLATILES CONTROL LEVEL 1 & 2 |
CLINICAL CONTROLS, INC. |
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