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FDA 510(k) Application Details - K963050
Device Classification Name
Handpiece, Air-Powered, Dental
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510(K) Number
K963050
Device Name
Handpiece, Air-Powered, Dental
Applicant
MIDWEST DENTAL PRODUCTS CORP.
901 W OAKTON ST.
DES PLAINES, IL 60018-1884 US
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HECTOR JIMENEZ-BILLINI
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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
08/06/1996
Decision Date
10/11/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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