BD ULTRA-FINE III PEN NEEDLE


Device Classification Name

needle, hypodermic, single lumen

510(k) Number K024109
Device Name BD ULTRA-FINE III PEN NEEDLE
Original Applicant
BECTON DICKINSON & CO.
1 becton dr.
franklin lakes, 
NJ 
07417 -1880

Original Contact john a schalgo
Regulation Number 880.5570
Classification Product Code
FMI  
Date Received 12/13/2002
Decision Date 12/30/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No