2009 H1n1 Influenza Virus (Swine Origin), Nucleic Acid Or Antigen, Detection And Identification
FDA product code OQW · 10 cleared devices
Class 2
Microbiology
- Regulation
- 21 CFR 866.3332
- Review panel
- MI
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2010-05-24 – 2013-08-26
2009 H1N1 influenza virus detection and identification reagents are used to directly detect and differentiate the 2009 H1N1 influenza virus in human respiratory specimens
OQW
2013-08-26
OQW
2013-05-22
CDC HUMAN INFLUENZA VIRUS REAL-TIME RT-PCR DIAGNOSTIC PANEL
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OQW
2013-01-14
CDC HUMAN INFLUENZA VIRUS REAL-TIME RT-PCR DIAGNOSTIC PANEL
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OQW
2012-05-18
XPERT FLU GENEXPERT DX SYSTEMS (GX-I, GX-IV)
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OQW
2011-09-13
JBAIDS INFLUENZA A SUBTYPING KIT
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OQW
2011-08-23
CDC HUMAN INFLUENZA VIRUS REAL-TIME RT-PCR DIAGNOSTIC PANEL
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OQW
2011-04-21
XPERT FLU, GENEXPERT DX SYSTEMS, GENEXPERT INFINITY SYSTEM, GENEXPERT SYSTEM SOFTWARE VERISIONS 2.1 AND 4.0
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OQW
2010-07-23
PROFAST+ ASSAY
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OQW
2010-06-22
CDC INFLUENZA 2009 A(H1N1)PDM REAL-TIME RT-PCR PANEL
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OQW
2010-05-24
SIMPLEXA INFLUENZA A H1N1 (2009) MODEL MOL2500
View details →No matching devices.
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