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FDA 510(k) Application Details - K082149
Device Classification Name
Sleeve, Limb, Compressible
More FDA Info for this Device
510(K) Number
K082149
Device Name
Sleeve, Limb, Compressible
Applicant
MEGO AFEK AC LTD
20 HATA'AS ST.
KFAR SABA 44425 IL
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Contact
AHAVA STEIN
Other 510(k) Applications for this Contact
Regulation Number
870.5800
More FDA Info for this Regulation Number
Classification Product Code
JOW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/30/2008
Decision Date
10/06/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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