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FDA 510(k) Applications Submitted by VICKIE J 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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