GREINER VACUETTE QUICKSHIELD COMPLETE


Device Classification Name

needle, hypodermic, single lumen

510(k) Number K072320
Device Name GREINER VACUETTE QUICKSHIELD COMPLETE
Applicant
GREINER BIO-ONE NORTH AMERICA, INC.
p.o. box 103
baldwin, 
MD 
21013

Applicant Contact judi smith
Correspondent
GREINER BIO-ONE NORTH AMERICA, INC.
p.o. box 103
baldwin, 
MD 
21013

Correspodent Contact judi smith
Regulation Number 880.5570
Classification Product Code
FMI  
Date Received 08/20/2007
Decision Date 09/14/2007
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

Recalls CDRH Recalls