FDA 510(k) Applications Submitted by THE KENDALL COMPANY DIV. OF TYCO HEALTHCARE GROUP
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K024010 | 12/04/2002 | DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETER | THE KENDALL COMPANY DIV. OF TYCO HEALTHCARE GROUP |
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