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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceMARGINPROBE SYSTEM
Generic NameDiagnostic low electric field
ApplicantDilon Medical Technologies, Ltd.
20 Alon Hatavor St.
P.O. Box 3131
Business Park-South 3088900 
PMA NumberP110014
Supplement NumberS002
Date Received01/28/2014
Decision Date05/15/2014
Product Code OEE 
Advisory Committee General & Plastic Surgery
Supplement TypeNormal 180 Day Track No User Fee
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL FOR A MANUFACTURING SITE LOCATED AT MEDIMOR LTD., IN TIBERIAS, ISRAEL (CONTRACT MANUFACTURER).
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