FDA 510(k) Application Details - K790599

Device Classification Name Instruments, Dental Hand

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510(K) Number K790599
Device Name Instruments, Dental Hand
Applicant HOWMEDICA CORP.

, US
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Regulation Number 872.4565

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Classification Product Code DZN
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Date Received 03/26/1979
Decision Date 05/21/1979
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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