FDA 510(k) Applications Submitted by IKONOS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K971252 04/03/1997 SEVRAIN CRANIAL CLAMP IKONOS CORP.
K971408 04/16/1997 SEVRAIN CRANIAL CLAMP (SCC-200 SERIES) IKONOS CORP.
K971454 04/21/1997 TYMPANOSTOMY VENTILATION TUBE IKONOS CORP.


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