FDA 510(k) Application Details - K140133

Device Classification Name Set, Administration, Intravascular

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510(K) Number K140133
Device Name Set, Administration, Intravascular
Applicant EMED TECHNOLOGIES CORPORATION
1264 Hawks Flight Ct Ste 200
EL DORADO HILLS, CA 95762 US
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Contact PETER KOLLINGS
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Regulation Number 880.5440

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Classification Product Code FPA
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Date Received 01/17/2014
Decision Date 05/15/2014
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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