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FDA 510(k) Application Details - K022217
Device Classification Name
Unit, Operative Dental
More FDA Info for this Device
510(K) Number
K022217
Device Name
Unit, Operative Dental
Applicant
ASEPTICO, INC.
8333 216TH ST., S.E.
WOODINVILLE, WA 98072 US
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Contact
GRANT RAMALEY
Other 510(k) Applications for this Contact
Regulation Number
872.6640
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Classification Product Code
EIA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/08/2002
Decision Date
10/24/2002
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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