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FDA 510(k) Application Details - K954790
Device Classification Name
Drill, Dental, Intraoral
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510(K) Number
K954790
Device Name
Drill, Dental, Intraoral
Applicant
TULSA DENTAL PRODUCTS, LTD.
5001 EAST 68TH ST.
TULSA, OK 74136 US
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Contact
RUSSELL VANDERSLICE
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Regulation Number
872.4130
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Classification Product Code
DZA
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More FDA Info for this Product Code
Date Received
10/19/1995
Decision Date
01/16/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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