FDA 510(k) Applications Submitted by COOPER SURGICAL

FDA 510(k) Number Submission Date Device Name Applicant
K023379 10/08/2002 COOPERSURGICAL EMBRYO TRANSFER CATHETER, COOPERSURGICAL ASSISTED REPRODUCTION CATHETER COOPER SURGICAL
K023382 10/08/2002 COOPERSURGICAL MALLEABLE SYTLET COOPER SURGICAL
K023383 10/08/2002 COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER COOPER SURGICAL
K023384 10/08/2002 COOPERSURGICAL TRIAL TRANSFER CATHETER COOPER SURGICAL
K091325 05/05/2009 TEN-YEAR FRACTURE RISK OPTION AND SIRI TABLE OPTION FOR NORLAND DXA BONE DENSITOMETERS COOPER SURGICAL


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