FDA 510(k) Applications Submitted by SUNMED, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K062112 07/24/2006 SUNMED FOLEY CATHETERS SUNMED, INC.
K955631 12/11/1995 ORTHOPLUG HARD BONE DESIGN SUNMED, INC.
K955632 12/11/1995 ORTHOPLUG SOFT BONE DESIGN SUNMED, INC.


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