Diamedix Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diamedix Corp. - FDA 510(k) Cleared Devices
68
Total
68
Cleared
0
Denied
Diamedix Corp. has 68 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 68 cleared submissions from 1986 to 2011. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Diamedix Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diamedix Corp.
68 devices
Cleared
Jan 21, 2011
MAGO 4S
Microbiology
477d
Cleared
Jul 09, 2002
DIAMEDIX IS-RHEUMATOID FACTOR TEST SYSTEM
Immunology
68d
Cleared
Jan 08, 2002
DIAMEDIX IS-ANTI-B2 GLYCOPROTEIN I SCREEN
Immunology
39d
Cleared
Dec 21, 2001
DIAMEDIX IS-ANTI-B2 GLYCOPROTEIN I IGG/IGM TEST SYSTEM
Immunology
46d
Cleared
Oct 26, 2001
DIAMEDIX IS-ANTI-CARDIOLIPIN IGG/IGM TEST SYSTEM
Immunology
86d
Cleared
Oct 26, 2001
DIAMEDIX IS-ANTI-CARDIOLIPIN IGA TEST SYSTEM
Immunology
86d
Cleared
Sep 28, 2001
DIAMEDIX IS-ANTI-GLIADIN IGG TEST SYSTEM
Immunology
38d
Cleared
Sep 28, 2001
DIAMEDIX IS-ANTI-GLIADIN IGA TEST SYSTEM
Immunology
38d
Cleared
Aug 20, 2001
DIAMEDIX IS-ANTI-CARDIOLIPIN SCREEN TEST SYSTEM
Immunology
49d
Cleared
Nov 28, 2000
DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM
Microbiology
126d
Cleared
Aug 21, 2000
DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM
Microbiology
62d
Cleared
Aug 07, 2000
DIAMEDIX IS-CMV IGM CAPTURE TEST SYSTEM
Microbiology
56d
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