Atlas FDA

Quantidex qPCR BCR-ABL IS Kit

FDA 510(k) clearance DEN160003 · decided 2016-07-22

Clearance details

K-number
DEN160003
Device name
Quantidex qPCR BCR-ABL IS Kit
Applicant
Asuragen, Inc.
Decision
Unknown
Date received
2016-01-19
Decision date
2016-07-22
Days to decision
185 days
Clearance type
Direct
Product code
OYX
Device class
2
Regulation number
866.6060
Medical specialty
Medical Genetics
Advisory committee
Medical Genetics
Location
Austin, TX, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
Fastplex™ BCR-ABL (p210) %IS digital PCR Kit (K252243)Suzhou Precigenome, Ltd. Co;2026-07-02
BCR-ABL1 (p210) % IS Kit (Digital PCR Method) (K221869)Suzhou Sniper Medical Technologies Co., Ltd.2023-09-05
Xpert BCR-ABL Ultra, GeneXpert Dx System, GeneXpert Infinity-48s and GeneXpert Infinity-80 Systems (K190076)Cepheid2019-09-27
QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System (K181661)Bio-Rad Laboratories, Inc.2019-02-13
MRDx BCR-ABL Test, MRDx BCR-ABL Test Software (K173492)Molecularmd Corporation2017-12-22

Recalls involving this device

No recalls on record reference this clearance.