Princeton Biomedix is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Princeton Biomedix - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Princeton Biomedix has 14 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1976 to 1995.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Princeton Biomedix
14 devices
Cleared
Feb 07, 1995
LIFESIGN MI MYOGLOBIN
Immunology
285d
Cleared
Jul 12, 1994
BIOSIGN(TM_ RUBELLA - RUBELLA ANTIBODY TEST
Microbiology
628d
Cleared
Mar 04, 1993
OVUSIGN LH/CONCEPTION PLUS/OVUDATE LH ONE-STEP
Chemistry
49d
Cleared
Feb 23, 1993
BIOSIGN(TM) MONO-INFECT MONO HETERO ANTIBODY TEST
Immunology
132d
Cleared
Jan 26, 1993
LIFESIGN HCG - ONE STEP HOME PREGNANCY TEST
Chemistry
42d
Cleared
May 04, 1990
BIOSIGN HCG-ONE STEP PREGNANCY TEST
Chemistry
60d
Cleared
Oct 18, 1989
BIOSPOT HCG-RAPID PREGNANCY TEST
Chemistry
85d
Cleared
Oct 18, 1989
BIOSTIX I. HCG - ONE STEP PREGNANCY TEST
Chemistry
84d
Cleared
Jun 19, 1989
BIOSTIX (TM)HCG--SIMPLE PREGNANCY TEST
Chemistry
67d
Cleared
Feb 24, 1977
ALKALINE PHOSPHATASE (ALP)/PNPP
Chemistry
63d
Cleared
Oct 27, 1976
TEST, LACTATE DEHYDROGENASE
Chemistry
86d
Cleared
Oct 27, 1976
ASSAY FOR GAMMA GLUTAMYLTRANSFERASE
Chemistry
86d
Cleared
Oct 05, 1976
SET, TRINDER GLUCOSE
Chemistry
64d
Cleared
Jul 20, 1976
TEST, ACID PHOSPHATASE
Chemistry
18d