FDA 510(k) Application Details - K955433

Device Classification Name Accessories, Catheter

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510(K) Number K955433
Device Name Accessories, Catheter
Applicant ALLIED BIOMEDICAL CORP.
3850 DR.
#C-2
PASO ROBLES, CA 93446 US
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Contact GERALD HANSON
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Regulation Number 878.4200

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Classification Product Code KGZ
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Date Received 11/28/1995
Decision Date 01/26/1996
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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