EZ REGULAR


Device Classification Name

set, administration, intravascular

510(k) Number K080303
Device Name EZ REGULAR
Applicant
MEINNTECH CO., LTD.
po box 7007
deerfield, 
IL 
60015

Applicant Contact daniel kamm
Correspondent
MEINNTECH CO., LTD.
po box 7007
deerfield, 
IL 
60015

Correspodent Contact daniel kamm
Regulation Number 880.5440
Classification Product Code
FPA  
Date Received 02/05/2008
Decision Date 08/05/2008
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