Atlas FDA

CAPTIA HSV 2 IGG TYPE SPECIFIC ELISA KIT

FDA 510(k) clearance K033106 · decided 2004-07-13

Clearance details

K-number
K033106
Device name
CAPTIA HSV 2 IGG TYPE SPECIFIC ELISA KIT
Applicant
Trinity Biotech USA
Decision
Substantially Equivalent
Date received
2003-09-30
Decision date
2004-07-13
Days to decision
287 days
Clearance type
Traditional
Product code
MYF
Device class
2
Regulation number
866.3305
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Jamestown, NY, US
Third-party review
No
Expedited review
No

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LIAISON HSV-2 TYPE SPECIFIC IGG ASSAY, CONTROL HSV-2 IGG (K081687)DiaSorin, Inc.2008-11-10
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Recalls involving this device

No recalls on record reference this clearance.