FDA 510(k) Application Details - K933455

Device Classification Name Unit, X-Ray, Intraoral

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510(K) Number K933455
Device Name Unit, X-Ray, Intraoral
Applicant SCHICK TECHNOLOGIES, INC.
30 NORTHPORT RD.
SOUND BEACH, NY US
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Contact RICHARD C LANZILLOTTO
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Regulation Number 872.1810

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Classification Product Code EAP
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Date Received 07/14/1993
Decision Date 01/31/1994
Decision SE - Substantially Equivalent
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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