Ameritek, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ameritek, Inc. - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Ameritek, Inc.
17 devices
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
Cleared
Mar 22, 1996
BEST PREGNANCY TEST
Chemistry
233d
Cleared
Oct 20, 1986
RK VACUUM FIXATION RING SYSTEM
Ophthalmic
24d
Cleared
Sep 25, 1986
SURGICAL IOP MONITOR
Ophthalmic
35d
Cleared
Mar 31, 1986
RARE EARTH INTRA-OCULAR MAGNET
Ophthalmic
18d
Cleared
Mar 31, 1986
ELECTRICALLY CONTROLLED I.V. POLE (OPTHALMIC)
Ophthalmic
13d