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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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