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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Delivery, Allergen And Vaccine
510(k) Number K020523
Device Name BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757
Applicant
BD
ONE BECTON DRIVE MC226
FRANKLIN LAKES,  NJ  07417
Applicant Contact PASQUALE AMOTO
Correspondent
BD
ONE BECTON DRIVE MC226
FRANKLIN LAKES,  NJ  07417
Correspondent Contact PASQUALE AMOTO
Classification Product Code
LDH  
Date Received02/19/2002
Decision Date 03/20/2002
Decision Substantially Equivalent (SESE)
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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