FDA 510(k) Applications Submitted by FLUIDSENSE CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K982170 06/19/1998 FLUIDSENSE FLUID DELIVERY SYSTEM FLUIDSENSE CORP.
K003582 11/20/2000 FLUIDSENSE FLUID DELIVERY SYSTEM MODEL FS-01 FLUIDSENSE CORP.


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