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510(k) K183414

ABSOLU by Quantel Medical — Product Code IYO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 20, 2019
Date Received
December 10, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Imaging, Pulsed Echo, Ultrasonic
Device Class
Class II
Regulation Number
892.1560
Review Panel
RA
Submission Type

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