Atlas FDA

ACCESS INTACT PTH AND CALIBRATORS, MODELS A 16972 AND A 16953

FDA 510(k) clearance K061190 · decided 2006-09-15

Clearance details

K-number
K061190
Device name
ACCESS INTACT PTH AND CALIBRATORS, MODELS A 16972 AND A 16953
Applicant
Beckman Coulter, Inc.
Decision
Substantially Equivalent
Date received
2006-04-28
Decision date
2006-09-15
Days to decision
140 days
Clearance type
Traditional
Product code
CEW
Device class
2
Regulation number
862.1545
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Chaska, MN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Access Intact PTH assay, a paramagnetic particle, chemiluminescent immunoassay for the qua recall (Z-0803-2025)Beckman Coulter, Inc.2025-01-03

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