510(k) K002989

PROCLUDE by Ortek Therapeutics, Inc. — Product Code EJR

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 14, 2000
Date Received
September 25, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Agent, Polishing, Abrasive, Oral Cavity
Device Class
Class I
Regulation Number
872.6030
Review Panel
DE
Submission Type