BD INTEGRA SYRINGE


Device Classification Name

syringe, piston

510(k) Number K023752
Device Name BD INTEGRA SYRINGE
Original Applicant
BD
one becton drive mc226
franklin lakes, 
NJ 
07417

Original Contact pasquale amato
Regulation Number 880.5860
Classification Product Code
FMF  
Subsequent Product Code
MEG  
Date Received 11/08/2002
Decision Date 02/07/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls