FDA 510(k) Application Details - K021378

Device Classification Name Unit, X-Ray, Extraoral With Timer

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510(K) Number K021378
Device Name Unit, X-Ray, Extraoral With Timer
Applicant DENTALEZ GROUP
1816 COLONIAL VILLAGE LN.
LANCASTER, PA 17601 US
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Contact DEON BECK
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Regulation Number 872.1800

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Classification Product Code EHD
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Date Received 05/01/2002
Decision Date 06/07/2002
Decision SESE - SUBST EQUIV
Classification Advisory Committee DE - Dental
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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