Atlas FDA

Lumipulse G B•R•A•H•M•S PCT Immunoreaction Cartridges, Lumipulse G B•R•A•H•M•S PCT Calibrators set

FDA 510(k) clearance K172713 · decided 2017-12-10

Clearance details

K-number
K172713
Device name
Lumipulse G B•R•A•H•M•S PCT Immunoreaction Cartridges, Lumipulse G B•R•A•H•M•S PCT Calibrators set
Applicant
Fujirebio Diagnostics,Inc.
Decision
Substantially Equivalent
Date received
2017-09-08
Decision date
2017-12-10
Days to decision
93 days
Clearance type
Traditional
Product code
PRI
Device class
2
Regulation number
866.3215
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Malvern, PA, 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
Dimension EXL LOCI BRAHMS Procalcitonin (PCT) (K220262)Siemens Healthcare Diagnostics, Inc.2022-08-26
Elecsys BRAHMS PCT (K192815)Roche Diagnostics2020-03-09
Elecsys BRAHMS PCT (K173927)Roche Diagnostics2018-07-06
LIAISON BRAHMS PCT II GEN, LIAISON Control BRAHMS PCT II GEN, LIAISON BRAHMS PCT II GEN Verifiers (K173683)DiaSorin, Inc.2018-02-27
ARCHITECT B.R.A.H.M.S PCT, ARCHITECT B.R.A.H.M.S PCT Calibrators, ARCHITECT B.R.A.H.M.S PCT Controls (K170652)Fisher Diagnostics2017-06-01
B R A H M S PCT sensitive KRYPTOR (K171338)Brahms GmbH2017-05-31
VIDAS B.R.A.H.M.S. PCT (PCT) (K162827)bioMerieux, Inc.2017-02-23

Recalls involving this device

No recalls on record reference this clearance.