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FDA 510(k) Applications Submitted by CANADA ENDOSCOPE CORPORATION
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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