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FDA 510(k) Application Details - K103689
Device Classification Name
System,X-Ray,Extraoral Source,Digital
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510(K) Number
K103689
Device Name
System,X-Ray,Extraoral Source,Digital
Applicant
PLANMECA OY
ASENTAJANKATU 6
HELSINKI FI-00880 FI
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Contact
LARS MORING
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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
12/17/2010
Decision Date
03/17/2011
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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