FDA 510(k) Application Details - K963112

Device Classification Name Set, Administration, Intravascular

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510(K) Number K963112
Device Name Set, Administration, Intravascular
Applicant MMG HEALTHCARE, INC.
5335 DIVIDEND DR.
DECATUR, GA 30034 US
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Contact JOHN H GOLDEN
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Regulation Number 880.5440

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Classification Product Code FPA
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Date Received 08/12/1996
Decision Date 11/08/1996
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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