Ameritek, Inc.
Ameritek, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2000.
Top product codes for Ameritek, Inc.
Recent clearances by Ameritek, Inc.
- K001215 — DBEST HCG 2 IU/ML TEST KIT
- K990873 — DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USE
- K990681 — DBSET MULTIDRUG SCREEN TEST KIT
- K984269 — DBEST OCCULT BLOOD TEST KIT
- K983188 — DBEST TETRAHYDROCANNABINOL TEST KIT
- K983189 — DBEST METHAMPHETAMINES TEST KIT
- K983190 — DBEST OPIATES TEST KIT
- K983191 — DBEST COCAINE TEST KIT
- K981504 — DBEST AMPHETAMINES TEST KIT
- K974508 — DBEST ONE-STEP OVULATION TEST
- K973957 — DBEST ONE-STEP HCG SERUM/URINE TEST
- K973142 — DBEST REAGENT STRIP FOR URINALYSIS
- K953606 — BEST PREGNANCY TEST
- K863775 — RK VACUUM FIXATION RING SYSTEM
- K863235 — SURGICAL IOP MONITOR
- K860960 — RARE EARTH INTRA-OCULAR MAGNET
- K861013 — ELECTRICALLY CONTROLLED I.V. POLE (OPTHALMIC)
Data sourced from openFDA. This site is unofficial and independent of the FDA.