510(k) K170524

Access AMH by Beckman Coulter, Inc. — Product Code PQO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 13, 2017
Date Received
February 22, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Anti-Müllerian Hormone Test System
Device Class
Class II
Regulation Number
862.1092
Review Panel
TX
Submission Type

An Anti-Müllerian hormone test system is an in vitro diagnostic device intended to measure anti-Müllerian hormone in human serum and plasma. The test is intended to be used as an aid for assessing ovarian reserve in women.