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FDA 510(k) Application Details - K070304
Device Classification Name
System,X-Ray,Extraoral Source,Digital
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510(K) Number
K070304
Device Name
System,X-Ray,Extraoral Source,Digital
Applicant
SOREDEX PALODEX GROUP OY
NAHKELANTIE 160
TUUSULA FIN-04300 FI
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Contact
KAI LANER
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Regulation Number
872.1800
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Classification Product Code
MUH
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More FDA Info for this Product Code
Date Received
01/31/2007
Decision Date
03/27/2007
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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