INTRAUTERINE DELIVERY SYSTEM – INJECTOR


Device Classification Name

cannula, manipulator/injector, uterine

510(k) Number K023051
Device Name INTRAUTERINE DELIVERY SYSTEM – INJECTOR
Original Applicant
PROSURG, INC.
2193 trade zone blvd.
san jose, 
CA 
95131

Original Contact ashvin desai
Classification Product Code
LKF  
Date Received 09/13/2002
Decision Date 12/12/2002
Decision

substantially equivalent

(SESE)

510k Review Panel

Obstetrics/Gynecology

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No