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510(k) K183428

Avulsion Forceps by STERIS Corporation — Product Code KGE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 16, 2019
Date Received
December 11, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, Biopsy, Electric
Device Class
Class II
Regulation Number
876.4300
Review Panel
GU
Submission Type

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