Atlas FDA

Solana Strep Complete Assay

FDA 510(k) clearance K162274 · decided 2016-10-25

Clearance details

K-number
K162274
Device name
Solana Strep Complete Assay
Applicant
Quidel Corporation
Decision
Substantially Equivalent
Date received
2016-08-12
Decision date
2016-10-25
Days to decision
74 days
Clearance type
Traditional
Product code
PGX
Device class
2
Regulation number
866.2680
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Athens, OH, US
Third-party review
No
Expedited review
No

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GenePOC Strep A (K183366)Genepoc, Inc.2019-03-06
Alere i Strep A 2, Alere i instrument, Alere i Strep A 2 Control Swab Kit (K173653)Alere Scarborough, Inc.2018-05-02
Xpert Xpress Strep A (K173398)Cepheid2018-04-26
ARIES Group A Strep Assay, ARIES Group A Strep Assay Protocol File Kit (K172402)Luminex Corporation2017-10-30
Xpert Xpress Strep A (K172126)Cepheid2017-09-25
Solana GAS Assay, Solana instrument (K150868)Quidel Corporation2015-06-23
ALERE I STREP A (K141757)Alere Scarborough, Inc.2015-03-31
Simplexa Group A Strep Direct, Simplexa Group A Strep Positive Control Pack (K143651)Focus Diagnostics, Inc.2015-03-18
LIAT STREP A ASSAY (K141338)Iquum, Inc.2014-11-04
AMPLIVUE GAS ASSAY (K141173)Quidel Corporation2014-07-24

Recalls involving this device

No recalls on record reference this clearance.