FDA 510(k) Applications Submitted by CHIRON VISION CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K960414 01/29/1996 SYNERGIST POWER PACK CHIRON VISION CORP.
K970727 02/28/1997 MPORT FOLDABLE LENS PLACEMENT SYSTEM CHIRON VISION CORP.
K972808 07/28/1997 HANSATOME MICROKERATOME CHIRON VISION CORP.


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