G-RINSE, MODEL 10031


Device Classification Name

media, reproductive

510(k) Number K022295
Device Name G-RINSE, MODEL 10031
Original Applicant
VITROLIFE SWEDEN AB
molndalsvagen 30
gothenburg, 

SE

se-412 63

Original Contact eiler anderson
Regulation Number 884.6180
Classification Product Code
MQL  
Date Received 07/16/2002
Decision Date 09/12/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Obstetrics/Gynecology

510k Review Panel

Obstetrics/Gynecology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No