FDA 510(k) Application Details - K913621

Device Classification Name Apron, Leaded

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510(K) Number K913621
Device Name Apron, Leaded
Applicant RINN DENTAL PRODUCTS
1212 ABBOTT DR.
ELGIN, IL US
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Contact RAYMOND G JACOBS
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Regulation Number 892.6500

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Classification Product Code EAJ
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Date Received 08/13/1991
Decision Date 09/27/1991
Decision SE - Substantially Equivalent
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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