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510(k) K200077

BioMin Restore Plus by Dr. Collins, Inc. — Product Code LBH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 6, 2020
Date Received
January 14, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Varnish, Cavity
Device Class
Class II
Regulation Number
872.3260
Review Panel
DE
Submission Type

Other clearances by Dr. Collins, Inc.

  • K181965 — Restore Toothpaste (June 13, 2019)

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