Diagnostic Hybrids, Inc. - FDA 510(k) Cleared Devices
37
Total
36
Cleared
1
Denied
Diagnostic Hybrids, Inc. has 36 FDA 510(k) cleared microbiology devices. Based in Athens, US.
Historical record: 36 cleared submissions from 1988 to 2010.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
37 devices
Not Cleared
May 13, 2014
QUIDEL MOLECULAR DIRECT HSV 1 +2/VZV ASSAY
Microbiology
81d
Cleared
May 18, 2010
THYRETAIN TM TSI REPORTER BIOASSAY
Immunology
299d
Cleared
Dec 23, 2009
D3 FASTPOINT L-DFA PARAINFLUENZA VIRUS/ADENOVIRUS IDENTIFICATION KIT
Microbiology
51d
Cleared
Dec 04, 2009
D3 FASTPOINT L-DFA RSV/MVP IDENTIFICATION KIT
Microbiology
51d
Cleared
Oct 21, 2009
D3 FASTPOINT L-DFA INFLUENZA A/INFLUENZA B VIRUS IDENTIFICATION KIT
Microbiology
33d
Cleared
Sep 11, 2009
D3 ULTRA DUET DFA RESPIRATORY VIRUS IDENTIFICATION KIT
Microbiology
142d
Cleared
Aug 28, 2009
ELVIS HSV ID AND D3 TYPING TEST SYSTEM
Microbiology
73d
Cleared
Aug 28, 2009
MODIFICATION TO D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT
Microbiology
30d
Cleared
May 21, 2009
THYROID STIMULATING IMMUNOGLOBULIN REPORTER ASSAY
Immunology
185d
Cleared
Mar 06, 2009
D3 DFA METAPNEUMOVIRUS IDENTIFICATION KIT
Microbiology
53d
Cleared
Dec 23, 2008
D3 DUET DFA INFLUENZA A/RESPIRATORY VIRUS SCREENING KIT
Microbiology
187d
Cleared
Dec 23, 2008
D3 DUET DFA RSV/RESPIRATORY VIRUS SCREENING KIT
Microbiology
169d
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