Light Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Light Diagnostics - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Light Diagnostics has 19 FDA 510(k) cleared microbiology devices. Based in Temecula, US.
Historical record: 19 cleared submissions from 1993 to 1999.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Light Diagnostics
19 devices
Cleared
Nov 09, 1999
LIGHT DIAGNOSTICS SIMULFLUOR HSV 1/2 IMMUNOFLUORECENCE ASSAY
Microbiology
160d
Cleared
Oct 19, 1999
LIGHT DIAGNOSTICS SIMULFLUOR HSV/VZV IMMUNOFLOURESCENCE ASSAY, MODEL 3295
Microbiology
273d
Cleared
Dec 22, 1998
LIGHT DIAGNOSTICS RABIES DFA REAGENT
Microbiology
498d
Cleared
Apr 08, 1998
LIGHT DIAGNOSTICS SIMULFLUOR FLU A/FLU B
Microbiology
142d
Cleared
Jun 07, 1996
CYTOMEGALOVIRUS DIRECT IMMUNOFLUORESCENCE ASSAY
Microbiology
414d
Cleared
Mar 20, 1996
VARICELLA-ZOSTER VIRUS DIRECT IMMUNOFLUORESCENCE ASSAY
Microbiology
336d
Cleared
Sep 12, 1995
POLIOVIRUS 3 MONOCLONAL ANTIBODY
Microbiology
616d
Cleared
Sep 12, 1995
POLIOVIRUS BLEND MONOCLONAL ANTIBODIES
Microbiology
617d
Cleared
Sep 12, 1995
POLIOVIRUS 2 MONOCLONAL ANTIBODY
Microbiology
616d
Cleared
Sep 08, 1995
COXSACKIEVIRUS B3 MONOCLONAL ANTIBODY
Microbiology
617d
Cleared
Sep 08, 1995
COXSACKIEVIRUS B@ MONOCLONAL ANTIBODY
Microbiology
617d
Cleared
Sep 08, 1995
COXSACKIEVIRUS B4 MONOCLONAL ANTIBODY
Microbiology
617d