ASP-100, MODEL 2100


Device Classification Name

media, reproductive

510(k) Number K991345
Device Name ASP-100, MODEL 2100
Applicant
VITROLIFE SWEDEN AB
molndalsvagen 30
gothenburg, 

SE

se-412 63

Applicant Contact eiler anderson
Correspondent
VITROLIFE SWEDEN AB
molndalsvagen 30
gothenburg, 

SE

se-412 63

Correspodent Contact eiler anderson
Regulation Number 884.6180
Classification Product Code
MQL  
Date Received 04/19/1999
Decision Date 02/18/2000
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