FDA 510(k) Application Details - K930321

Device Classification Name Syringe, Piston

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510(K) Number K930321
Device Name Syringe, Piston
Applicant BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
1 BECTON DR.
FRANKLIN LAKES, NJ US
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Contact GREGORY W MORGAN
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Regulation Number 880.5860

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Classification Product Code FMF
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Date Received 01/22/1993
Decision Date 05/17/1993
Decision SE - Substantially Equivalent
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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