Atlas FDA

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

FDA 510(k) clearance K173798 · decided 2018-03-14

Clearance details

K-number
K173798
Device name
Simplexa HSV 1 & 2 Direct, Simplexa HSV 1 & 2 Positive Control Pack
Applicant
Diasorin Molecular, LLC
Decision
Substantially Equivalent
Date received
2017-12-14
Decision date
2018-03-14
Days to decision
90 days
Clearance type
Traditional
Product code
PGI
Device class
2
Regulation number
866.3309
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
Alinity m HSV 1 & 2 / VZV (K233349)Abbott Molecular, Inc.2024-05-03
Savanna HSV 1+2/VZV Assay, Savanna HSV 1+2/VZV Control Set, Savanna Instrument (K232286)Quidel Corporation2023-12-20
Simplexa VZV Swab Direct, Simplexa VZV Positive Control Pack (K192376)Diasorin Molecular, LLC2019-11-26
HSV 1 & 2 ELITe MGB Kit; ELITe InGenius (K180559)Elitechgroup2018-10-29
Solana HSV 1+2/VZV Assay (K162451)Quidel Corporation2016-11-28
ARIES HSV 1&2 Assay Cassettes - Carton of 24 (IVD), ARIES HSV 1&2 Assay Protocol File Kit (IVD), ARIES HSV 1&2 Assay Cassette (IVD) (K151906)Luminex Corporation2015-10-06
illumigene HSV 1&2 DNA Amplification Assay, illumigene HSV 1&2 External Control Kit, illumipro-10 (K151046)Meridian Bioscience, Inc.2015-07-17
QUIDEL MOLECULAR DIRECT HSV 1 +2/VZV ASSAY (DEN140004)Diagnostic Hybrids, Inc.2014-05-13

Recalls involving this device

No recalls on record reference this clearance.