Pb Diagnostic Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pb Diagnostic Systems, Inc. - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
Pb Diagnostic Systems, Inc. has 35 FDA 510(k) cleared medical devices. Based in Westwood, US.
Historical record: 35 cleared submissions from 1988 to 1994. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Pb Diagnostic Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pb Diagnostic Systems, Inc.
35 devices
Cleared
Jul 28, 1994
OPUS FT4 TEST SYSTEM
Chemistry
176d
Cleared
Jul 20, 1994
OPUS PROCAINAMIDE TEST SYSTEM
Toxicology
289d
Cleared
Jun 28, 1994
OPUS CMV-G
Microbiology
351d
Cleared
Mar 07, 1994
OPUS(R) SEROLOGY CONTROLS, MODIFICATION
Microbiology
194d
Cleared
Dec 22, 1993
OPUS DIGITOXIN
Toxicology
51d
Cleared
Nov 22, 1993
OPUS NAPA
Toxicology
53d
Cleared
Sep 08, 1993
OPUS ESTRADIOL
Chemistry
78d
Cleared
Sep 08, 1993
OPUS TOTAL CK
Chemistry
42d
Cleared
Jul 08, 1993
OPUS(R) TOTAL B-HCG TEST SYSTEM
Chemistry
57d
Cleared
Jun 07, 1993
OPUS MAGNUM ANALYZER
Chemistry
182d
Cleared
Dec 11, 1992
OPUS(R) VANCOMYCIN
Toxicology
72d
Cleared
Oct 15, 1992
OPUS(R) CK-MB
Toxicology
44d