Val Tech Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Val Tech Diagnostics, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Val Tech Diagnostics, Inc. has 11 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 11 cleared submissions from 1987 to 1988. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Val Tech Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Val Tech Diagnostics, Inc.
11 devices
Cleared
Oct 06, 1988
HISTO-CHECK LEGIONELLA CONTROL SLIDES
Microbiology
45d
Cleared
Oct 06, 1988
HISTO-CHECK ACID FAST SLIDES
Microbiology
45d
Cleared
Oct 06, 1988
HISTO-CHECK GRAM NEGATIVE SLIDES
Microbiology
45d
Cleared
Oct 06, 1988
HISTO-CHECK FUNGAL CONTROL SLIDES
Microbiology
45d
Cleared
Oct 06, 1988
HISTO-CHECK PARASITIC CONTROL SLIDES
Microbiology
45d
Cleared
Sep 28, 1988
HERPES VIRUS CONTROL SLIDES
Microbiology
30d
Cleared
Sep 07, 1988
HISTONE REACTIVE ANA
Immunology
37d
Cleared
Aug 25, 1988
HISTO-CHECK SLIDES
Microbiology
27d
Cleared
Apr 20, 1987
DUAL SUBSTRATE ANA
Immunology
13d
Cleared
Mar 12, 1987
ANA TEST KIT
Immunology
100d
Cleared
Mar 10, 1987
RAT LIVER NUCLEI TEST SYSTEM
Immunology
13d