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510(k) K993556

LIQUIBAND DENTAL by Medlogic Global Corp. — Product Code EMA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 3, 2000
Date Received
October 20, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cement, Dental
Device Class
Class II
Regulation Number
872.3275
Review Panel
DE
Submission Type

Other clearances by Medlogic Global Corp.

  • K083531 — LIQUIBAND ULTIMA, MODEL LB0004 (February 12, 2009)
  • K972081 — SUPERSKIN (December 17, 1997)

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