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510(k) Premarket Notification Database

Device Classification Name:	DELIVERY SYSTEM, ALLERGEN AND VACCINE
Regulation Number:	[See Other Products with this regulation number]
510(k) Number:	K032528
Device Name:	BD ECLIPSE BIFURCATED NEEDLE
Applicant:	BECTON DICKINSON & CO. 1 BECTON DR. FRANKLIN LAKES, NJ 07417 1885
Contact:	PETER ZURLO
Product Code:	LDH [See Other Manufacturers that make this Product]
Date Received:	08-15-2003
Decision Date:	09-09-2003
Decision:	SE
Advisory Committee:	HO
Statement/Summary/Purged Status:	Statement
Type:	Special
Review by Third Party:	N
Expedited Review:	N

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