FDA 510(k) Applications Submitted by AMERITEK, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K953606 |
08/02/1995 |
BEST PREGNANCY TEST |
AMERITEK, INC. |
K983188 |
09/11/1998 |
DBEST TETRAHYDROCANNABINOL TEST KIT |
AMERITEK, INC. |
K983189 |
09/11/1998 |
DBEST METHAMPHETAMINES TEST KIT |
AMERITEK, INC. |
K983190 |
09/11/1998 |
DBEST OPIATES TEST KIT |
AMERITEK, INC. |
K983191 |
09/11/1998 |
DBEST COCAINE TEST KIT |
AMERITEK, INC. |
K973957 |
10/16/1997 |
DBEST ONE-STEP HCG SERUM/URINE TEST |
AMERITEK, INC. |
K984269 |
10/22/1998 |
DBEST OCCULT BLOOD TEST KIT |
AMERITEK, INC. |
K990681 |
03/02/1999 |
DBSET MULTIDRUG SCREEN TEST KIT |
AMERITEK, INC. |
K990873 |
03/16/1999 |
DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USE |
AMERITEK, INC. |
K001215 |
04/14/2000 |
DBEST HCG 2 IU/ML TEST KIT |
AMERITEK, INC. |
K981504 |
04/27/1998 |
DBEST AMPHETAMINES TEST KIT |
AMERITEK, INC. |
K973142 |
08/21/1997 |
DBEST REAGENT STRIP FOR URINALYSIS |
AMERITEK, INC. |
K974508 |
12/01/1997 |
DBEST ONE-STEP OVULATION TEST |
AMERITEK, INC. |
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