FDA 510(k) Application Details - K870563

Device Classification Name Apron, Leaded

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510(K) Number K870563
Device Name Apron, Leaded
Applicant X-TECH, LTD.
P.O. BOX 6069
NEWBURYPORT, MA US
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Contact PRESTON GILL
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Regulation Number 892.6500

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Classification Product Code EAJ
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Date Received 02/10/1987
Decision Date 02/19/1987
Decision SE - Substantially Equivalent
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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