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FDA 510(k) Application Details - K991239
Device Classification Name
Scaler, Ultrasonic
More FDA Info for this Device
510(K) Number
K991239
Device Name
Scaler, Ultrasonic
Applicant
MICRON CORP.
1-34-14 HIGASHIYUKIGAYA
OHTA-KU, TOKYO 145-0065 JP
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Contact
EIJI SUZUKI
Other 510(k) Applications for this Contact
Regulation Number
872.4850
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Classification Product Code
ELC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/12/1999
Decision Date
10/18/1999
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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