Atlas FDA

SeraQuest HSV Type 2 Specific IgG

FDA 510(k) clearance K181514 · decided 2019-06-13

Clearance details

K-number
K181514
Device name
SeraQuest HSV Type 2 Specific IgG
Applicant
Quest International, Inc.
Decision
Substantially Equivalent
Date received
2018-06-08
Decision date
2019-06-13
Days to decision
370 days
Clearance type
Traditional
Product code
MYF
Device class
2
Regulation number
866.3305
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Palm City, FL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Quest International

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls (K243575)Biokit, S.A.2025-02-12
Elecsys HSV-2 IgG (08948887160) (K220924)Roche Diagnostics2022-10-12
ADVIA Centaur Herpes-2 IgG (K181334)Biokit, S.A.2018-08-23
SeraQuest HSV Type 2 Specific IgG (K152353)Quest International, Inc.2016-05-13
ZEUS ELISA HSV GG-2 IGG TEST SYSTEM (K103603)Zeus Scientific, Inc.2011-05-20
LIAISON HSV-2 TYPE SPECIFIC IGG ASSAY, CONTROL HSV-2 IGG (K081687)DiaSorin, Inc.2008-11-10
EUROIMMUN ANTI-HSV-2 ELISA (IGG) AND ANTI-HSV-1 ELISA (IGG) KIT (K061239)Euroimmun Us, LLC2007-06-28
CAPTIA HSV 2 IGG TYPE SPECIFIC ELISA KIT (K033106)Trinity Biotech USA2004-07-13
HSV-2 ELISA IGG, MODEL EL0920G (K993724)Mrl Diagnostics2000-02-01

Recalls involving this device

No recalls on record reference this clearance.