Atlas FDA

VITEK REVEAL GN AST Assay and VITEK REVEAL AST System

FDA 510(k) clearance K260160 · decided 2026-07-08

Clearance details

K-number
K260160
Device name
VITEK REVEAL GN AST Assay and VITEK REVEAL AST System
Applicant
bioMerieux, Inc.
Decision
Substantially Equivalent
Date received
2026-01-20
Decision date
2026-07-08
Days to decision
169 days
Clearance type
Traditional
Product code
SAN
Device class
2
Regulation number
866.1650
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Hazelwood, MO, 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.

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PhAST instrument and PhAST Blood Culture Gram-negative Panel (K253316)Phast Corp.2026-06-26
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VITEK REVEAL GN AST Assay and VITEK REVEAL AST System (K230675)Specific Diagnostics, LLC2024-06-20
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LifeScale Gram Negative Kit (LSGN) with the LifeScale AST System (K211815)Affinity Biosensors2024-04-02

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
THXID™-BRAF (P120014/S012)bioMerieux, Inc.2021-12-20
THxID-BRAF kit (P120014/S011)bioMerieux, Inc.2021-03-10
THxID-BRAF assay kit (P120014/S010)bioMerieux, Inc.2020-02-26
THxID BRAF assay kit (P120014/S009)bioMerieux, Inc.2019-08-26
THxID BRAF assay kit (P120014/S008)bioMerieux, Inc.2018-06-27
THxID-BRAF kit (P120014/S007)bioMerieux, Inc.2016-11-22
VIDAS TOTAL PSA (P040008/S013)bioMerieux, Inc.2016-05-31
THXID-BRAF KIT (P120014/S006)bioMerieux, Inc.2016-04-05