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FDA 510(k) Application Details - K954722
Device Classification Name
Handpiece, Air-Powered, Dental
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510(K) Number
K954722
Device Name
Handpiece, Air-Powered, Dental
Applicant
NOUVAG AG
555 THIRTEEN ST., N.W.
WASHINGTON, DC 20004 US
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Contact
HOWARD M HOLSTEIN
Other 510(k) Applications for this Contact
Regulation Number
872.4200
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Classification Product Code
EFB
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More FDA Info for this Product Code
Date Received
10/13/1995
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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