Medical Device Manufacturer · US , Miami , FL

Ameritek, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1986

17

Total

17

Cleared

0

Denied

Ameritek, Inc. has 17 FDA 510(k) cleared medical devices. Based in Miami, US.

Historical record: 17 cleared submissions from 1986 to 2000.

Browse the FDA 510(k) cleared devices submitted by Ameritek, Inc. Filter by specialty or product code using the sidebar.

Ameritek, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ameritek, Inc.

17 devices

1-12 of 17

Cleared Jun 22, 2000

DBEST HCG 2 IU/ML TEST KIT

Chemistry · 69d

Cleared Sep 01, 1999

DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USE

Chemistry · 169d

Cleared Jul 15, 1999

DBSET MULTIDRUG SCREEN TEST KIT

Toxicology · 135d

Cleared May 11, 1999

DBEST OCCULT BLOOD TEST KIT

Hematology · 201d

Cleared Nov 18, 1998

DBEST TETRAHYDROCANNABINOL TEST KIT

Toxicology · 68d

Cleared Nov 18, 1998

DBEST METHAMPHETAMINES TEST KIT

Toxicology · 68d

Cleared Nov 18, 1998

DBEST OPIATES TEST KIT

Toxicology · 68d

Cleared Nov 18, 1998

DBEST COCAINE TEST KIT

Toxicology · 68d

Cleared Aug 06, 1998

DBEST AMPHETAMINES TEST KIT

Toxicology · 101d

Cleared Feb 02, 1998

DBEST ONE-STEP OVULATION TEST

Chemistry · 63d

Cleared Dec 17, 1997

DBEST ONE-STEP HCG SERUM/URINE TEST

Chemistry · 62d

Cleared Oct 20, 1997

DBEST REAGENT STRIP FOR URINALYSIS

Chemistry · 60d