FDA 510(k) Application Details - K760985

Device Classification Name Broach, Endodontic

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510(K) Number K760985
Device Name Broach, Endodontic
Applicant ADP INTL., INC.

, US
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Regulation Number 872.4565

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Classification Product Code EKW
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Date Received 10/21/1976
Decision Date 11/15/1976
Decision SE - Substantially Equivalent
Classification Advisory Committee DE - Dental
Review Advisory Committee DE - Dental
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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