FDA 510(k) Applications Submitted by ROGER LECLERC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093725 | 12/03/2009 | CYSTOSCOPE, MODELS CE0004-C, CE006-C, CE3004-C, CE3027-C, CE7004-C, CE1204-C, CE1227-C | CANADA ENDOSCOPE CORPORATION |
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