Ameritek, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Known Names

ameritek, ameri-tek

Recent 510(k) Clearances

K-NumberDeviceDate
K001215DBEST HCG 2 IU/ML TEST KITJune 22, 2000
K990873DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USESeptember 1, 1999
K990681DBSET MULTIDRUG SCREEN TEST KITJuly 15, 1999
K984269DBEST OCCULT BLOOD TEST KITMay 11, 1999
K983189DBEST METHAMPHETAMINES TEST KITNovember 18, 1998
K983191DBEST COCAINE TEST KITNovember 18, 1998
K983188DBEST TETRAHYDROCANNABINOL TEST KITNovember 18, 1998
K983190DBEST OPIATES TEST KITNovember 18, 1998
K981504DBEST AMPHETAMINES TEST KITAugust 6, 1998
K974508DBEST ONE-STEP OVULATION TESTFebruary 2, 1998
K973957DBEST ONE-STEP HCG SERUM/URINE TESTDecember 17, 1997
K973142DBEST REAGENT STRIP FOR URINALYSISOctober 20, 1997
K953606BEST PREGNANCY TESTMarch 22, 1996
K863775RK VACUUM FIXATION RING SYSTEMOctober 20, 1986
K863235SURGICAL IOP MONITORSeptember 25, 1986
K861013ELECTRICALLY CONTROLLED I.V. POLE (OPTHALMIC)March 31, 1986
K860960RARE EARTH INTRA-OCULAR MAGNETMarch 31, 1986