Atlas FDA

Access AMH

FDA 510(k) clearance K170524 · decided 2017-11-13

Clearance details

K-number
K170524
Device name
Access AMH
Applicant
Beckman Coulter, Inc.
Decision
Substantially Equivalent
Date received
2017-02-22
Decision date
2017-11-13
Days to decision
264 days
Clearance type
Traditional
Product code
PQO
Device class
2
Regulation number
862.1092
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Chaska, MN, 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
ADVIA Centaur® Anti-Müllerian Hormone (AMH) (K221801)Siemens Healthcare Diagnostics, Inc.2023-06-02
Access AMH (K223679)Beckman Coulter, Inc.2023-02-03
Elecsys AMH (K203757)Roche Diagnostics2022-06-10
Elecsys AMH, AMH CalSet, PreciControl AMH, AMH CalCheck 5 (DEN150057)Roche Diagnostics2016-12-19

Recalls involving this device

No recalls on record reference this clearance.

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