PROMOTOR


Device Classification Name

media, reproductive

510(k) Number K023106
Device Name PROMOTOR
Original Applicant
CERES FERTILITY, INC.
3722 ave. sausalito
irvine, 
CA 
92606

Original Contact grace holland
Regulation Number 884.6180
Classification Product Code
MQL  
Date Received 09/18/2002
Decision Date 11/05/2002
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