THE DIVACUP MENSTRUAL SOLUTION


Device Classification Name

cup, menstrual

510(k) Number K021356
Device Name THE DIVACUP MENSTRUAL SOLUTION
Original Applicant
DIVA INTERNATIONAL INC
p.o. box 25089
1375 weber street e
kitchener ontario, 

CA

n2a 4a5

Original Contact francine chambers
Regulation Number 884.5400
Classification Product Code
HHE  
Date Received 04/29/2002
Decision Date 07/16/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Obstetrics/Gynecology

510k Review Panel

Obstetrics/Gynecology

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No