Atlas FDA

Simplexa HSV 1 & 2 Direct, Simplexa HSV 1 & 2 Positive Control Pack

FDA 510(k) clearance K150962 · decided 2015-08-28

Clearance details

K-number
K150962
Device name
Simplexa HSV 1 & 2 Direct, Simplexa HSV 1 & 2 Positive Control Pack
Applicant
Focus Diagnostics
Decision
Substantially Equivalent
Date received
2015-04-10
Decision date
2015-08-28
Days to decision
140 days
Clearance type
Traditional
Product code
OQO
Device class
2
Regulation number
866.3305
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Cypress, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Sentosa SA201 HSV 1/2 Qualitative PCR Test (K172509)Vela Diagnostics USA, Inc.2018-02-01
Aptima Herpes Simplex Viruses 1 & 2 Assay (K162673)Hologic, Inc.2017-06-15
cobas HSV 1 and 2 Test (K150617)Roche Molecular Systems, Inc.2015-06-01
SEEGENE ANYPLEX II HSV-1/2 ASSAY (K142156)Seegene2015-02-13
artus HSV-1/2 QS-RGQ MDx Kit (K142738)Qiagen2014-12-19
IMDX HSV-1/2 FOR ABBOTT M2000 (K140198)Intelligent Medical Devices, Inc.2014-05-13
AMIPLIVUE HSV 1&2 ASSAY (K140029)Quidel Corporation2014-03-26
ISOAMP HSV ASSAY (K111951)Biohelix Corporation2011-09-27
MULTICODE-RTX HERPES SIMPLEX VIRUS 1 & 2 KIT (K111527)Eragen Biosciences, Inc.2011-08-03
BD PROBETEC HERPES SIMPLEX VIRUSES (HSV 1& 2) Q AMPLIFIED DNA ASSAYS (K103798)Becton, Dickinson & CO2011-03-18
MULTICODE - RTX HERPES SIMPLEX VIRUS 1 AND 2 KIT, MODEL 3711 (K100336)Eragen Biosciences2010-05-12

Recalls involving this device

RecordFirmDate
MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Mucocutaneous Swabs Produc recall (Z-2547-2020)DiaSorin Molecular LLC2020-07-10
Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451, MOL1452, MOL145 recall (Z-1272-2016)Focus Diagnostics Inc2016-04-02