Ampcor, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ampcor, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Ampcor, Inc. has 15 FDA 510(k) cleared medical devices. Based in Bridgeport, US.
Historical record: 15 cleared submissions from 1988 to 1992. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Ampcor, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ampcor, Inc.
15 devices
Cleared
Jul 14, 1992
IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TEST
Immunology
60d
Cleared
Jul 14, 1992
INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TEST
Immunology
60d
Cleared
Sep 13, 1991
DIPSTICK SALMONELLA
Microbiology
225d
Cleared
Aug 21, 1989
SINGLE AND DUAL BAND DIPSTICK HCG TEST
Chemistry
87d
Cleared
Jun 09, 1989
QUIK-DOT TOXOPLASMOSIS
Microbiology
154d
Cleared
Apr 14, 1989
QUIK-DOT C REACTIVE PROTEIN
Immunology
14d
Cleared
Apr 14, 1989
C REACTIVE PROTEIN LIQUID
Immunology
14d
Cleared
Jan 31, 1989
QUIK-DOT ANTISTREPTOLYSIN-O
Microbiology
27d
Cleared
Dec 22, 1988
GROUP A STREP, BETA-STREP
Microbiology
38d
Cleared
May 17, 1988
PREGNANCY (HCG) CARD & LIQUID TEST
Chemistry
125d
Cleared
Apr 28, 1988
PREGNANCY BETA-HCG CARD & LIQUID TEST
Chemistry
84d
Cleared
Mar 30, 1988
TRUST RPR TEST FOR SYPHILIS IN SERUM OR PLASMA
Microbiology
77d