Atlas FDA

ACCESS OSTASE QC

FDA 510(k) clearance K994277 · decided 2000-01-14

Clearance details

K-number
K994277
Device name
ACCESS OSTASE QC
Applicant
Beckman Coulter, Inc.
Decision
Substantially Equivalent
Date received
1999-12-20
Decision date
2000-01-14
Days to decision
25 days
Clearance type
Traditional
Product code
JJX
Device class
1
Regulation number
862.1660
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Access Ostase QC, Part Number: 37309. The Access Ostase QC is intended for monitoring syst recall (Z-1239-2012)Beckman Coulter Inc.2012-03-21
Access Immunoassay Systems Quality Control Kits, Part Number: 37309 The Access Ostase QC i recall (Z-2606-2011)Beckman Coulter Inc.2011-06-21

PMA approvals by this applicant

RecordFirmDate
Access AFP (on DxI 9000 Analyzer) (P980041/S051)Beckman Coulter, Inc.2025-11-03
Access HBsAg, Access HBsAg Confirmatory, Access HBsAg Calibrator, Access HBsAg QC (P230015)Beckman Coulter, Inc.2025-10-17
Access Hybritech p2PSA (P090026/S032)Beckman Coulter, Inc.2025-06-16
Access Hybritech free PSA (P970038/S046)Beckman Coulter, Inc.2025-05-15
Access Hybritech PSA (P850048/S060)Beckman Coulter, Inc.2024-09-04
Access Hybritech PSA reagent pack (P850048/S059)Beckman Coulter, Inc.2023-05-25
Access AFP Reagents on the Access Immunoassay Systems (P980041/S050)Beckman Coulter, Inc.2022-12-16
Access Hybritech PSA Reagents on the Access Immunoassay Systems (P850048/S057)Beckman Coulter, Inc.2022-12-16