FDA 510(k) Application Details - K051499

Device Classification Name Set, Administration, Intravascular

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510(K) Number K051499
Device Name Set, Administration, Intravascular
Applicant MEDEGEN MEDICAL MANUFACTURING SERVICES
15 CHEROKEE
TRABUCO CANYON, CA 92679 US
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Contact SALVADORE F PALOMARES
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Regulation Number 880.5440

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Classification Product Code FPA
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Date Received 06/07/2005
Decision Date 06/22/2005
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 Y
Expedited Review



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