Atlas FDA

CREATININE

FDA 510(k) clearance K061193 · decided 2006-06-23

Clearance details

K-number
K061193
Device name
CREATININE
Applicant
Abbott Laboratories, Inc.
Decision
Substantially Equivalent
Date received
2006-04-28
Decision date
2006-06-23
Days to decision
56 days
Clearance type
Traditional
Product code
CGX
Device class
2
Regulation number
862.1225
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Irving, TX, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ARCHITECT AUSAB; Alinity i Anti-HBs (P050051/S061)Abbott Laboratories, Inc.2025-04-03
ARCHITECT AUSAB/Alinity i Anti-HBs (P050051/S060)Abbott Laboratories, Inc.2024-05-23
ARCHITECT AUSAB / Alinity i Anti-HBs (P050051/S059)Abbott Laboratories, Inc.2024-03-22
ARCHITECT AUSAB (P050051/S050)Abbott Laboratories, Inc.2024-01-19
ARCHITECT AUSAB / Alinity i Anti-HBs (P050051/S058)Abbott Laboratories, Inc.2023-12-14
ARCHITECT AUSAB, Alinity i Anti-HBs (P050051/S057)Abbott Laboratories, Inc.2023-12-07
Alinity i Anti-HBs Reagent Kit (2x 100 Tests), Alinity i Anti-HBs Reagent Kit (2x600 Tests), Alinity i Anti-HBs Reagent (P050051/S056)Abbott Laboratories, Inc.2023-11-06
Alinity i Anti-HBs Reagent Kit (2x100 Tests), Alinity i Anti-HBs Reagent Kit (2x600 Tests), Alinity i Anti-HBs Reagent K (P050051/S055)Abbott Laboratories, Inc.2023-11-03