Lmd Laboratories is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lmd Laboratories - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Lmd Laboratories has 12 FDA 510(k) cleared microbiology devices. Based in San Diego, US.
Historical record: 12 cleared submissions from 1984 to 1996.
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 - Lmd Laboratories
12 devices
Cleared
Jun 07, 1996
LMD CRYPTOSPORIDIUM ANTIGEN DETECTION
Microbiology
199d
Cleared
Sep 27, 1995
E. COLI 0157 ELISA STOOL ASSAY
Microbiology
476d
Cleared
Jun 22, 1995
LMD GIARDIA ANTIGEN DETECTION ASSAY
Microbiology
262d
Cleared
Sep 05, 1991
CRYPTOSPORIDIUM ANTIGEN DETECTION
Microbiology
266d
Cleared
Mar 21, 1991
TRICHINELLA SEROLOGY MICROTITER ELISA
Microbiology
161d
Cleared
Oct 04, 1990
CYSTICERCOSIS SEROLOGICAL REAGENTS
Microbiology
226d
Cleared
Mar 14, 1989
GIARDIA STOOL ANTIGEN TEST KIT
Microbiology
70d
Cleared
Jan 24, 1989
TREND(R) EMERGE(TM) TOXOPLASMA IGG ELISA
Microbiology
146d
Cleared
Aug 11, 1987
AMEBIASIS ELISA TEST KIT
Microbiology
195d
Cleared
Nov 12, 1985
MEBIASIS AGAR GEL DIFFUSION KIT
Microbiology
22d
Cleared
Oct 22, 1985
ENTAMOEBA HISTOLYTICA-POSITIVE CONTROL(RABBIT)
Microbiology
22d
Cleared
Dec 06, 1984
ENTAMOEBA HISTOLYTICA HK-9 ANTIGEN (AXENIC)
Microbiology
44d