Atlas FDA

Elecsys AMH

FDA 510(k) clearance K203757 · decided 2022-06-10

Clearance details

K-number
K203757
Device name
Elecsys AMH
Applicant
Roche Diagnostics
Decision
Substantially Equivalent
Date received
2020-12-23
Decision date
2022-06-10
Days to decision
534 days
Clearance type
Traditional
Product code
PQO
Device class
2
Regulation number
862.1092
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Indianapolis, IN, 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
Access AMH (K170524)Beckman Coulter, Inc.2017-11-13
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
Elecsys Anti-HBs II, PreciControl Anti-HBs (P190034/S010)Roche Diagnostics2025-05-22
Elecsys Anti-HBe (P190005/S007)Roche Diagnostics2025-05-22
Elecsys Anti-HBe (P190005/S006)Roche Diagnostics2024-10-03
Elecsys Anti-HBs / Elecsys HBs II (P190034/S009)Roche Diagnostics2024-10-03
Elecsys Anti-HBs II (P190034/S008)Roche Diagnostics2024-08-29
Elecsys Anti-HBe (P190005/S005)Roche Diagnostics2024-08-29
Elecsys Anti-HBs II, PreciControl Anti-HBs (P190034/S007)Roche Diagnostics2024-07-23
Elecsys Anti-HBs II, PreciControl Anti-HBs (P190034/S005)Roche Diagnostics2024-05-01