FDA 510(k) Applications Submitted by WRIGHT LINEAR PUMP, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K071040 04/12/2007 WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMS WRIGHT LINEAR PUMP, INC.
K961292 04/04/1996 WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIAL WRIGHT LINEAR PUMP, INC.
K961797 05/09/1996 WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITE WRIGHT LINEAR PUMP, INC.
K961891 05/09/1996 WLP SINGLE-SEGMENT VERSION WLP SOLO VII WRIGHT LINEAR PUMP, INC.


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