FDA 510(k) Applications Submitted by PAUSCH CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K973834 10/08/1997 CS2000 & CS2000 TOMO PAUSCH CORP.
K973864 10/09/1997 COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMO PAUSCH CORP.


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