FDA 510(k) Applications Submitted by VICKIE BRADY

FDA 510(k) Number Submission Date Device Name Applicant
K012061 07/02/2001 SUPERIOR BATH, MODEL 6300 PENNER MANUFACTURING, INC.
K040772 03/26/2004 PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEM PENNER MANUFACTURING, INC.
K012057 07/02/2001 CASCADE BATH, MODEL 6900 PENNER MANUFACTURING, INC.


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