FDA 510(k) Applications Submitted by CORTEK ENDOSCOPY, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000197 | 01/21/2000 | CORTEK CYSTOSCOPE | CORTEK ENDOSCOPY, INC. |
| K000198 | 01/21/2000 | CORTEK ARTHROSCOPE | CORTEK ENDOSCOPY, INC. |
| K000199 | 01/21/2000 | CORTEK MINI LAPAROSCOPE | CORTEK ENDOSCOPY, INC. |
| K000200 | 01/21/2000 | CORTEK URETHEROSCOPE | CORTEK ENDOSCOPY, INC. |
| K000202 | 01/21/2000 | CORTEK LAPAROSCOPES | CORTEK ENDOSCOPY, INC. |
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