FDA 510(k) Applications Submitted by COVIDIEN LLC, FORMERLY REGISTERED AS TYCO HEALTHCA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K102605 | 09/10/2010 | MAHURKAR TRIPLE LUMEN DIALYSIS CATHETER | COVIDIEN LLC, FORMERLY REGISTERED AS TYCO HEALTHCA |
| K102325 | 08/17/2010 | IDRIVE SYSTEM (I DRIVE POWER HANDLE, IDRIVE (RALC) SINGLE USE RELOAD) | COVIDIEN LLC, FORMERLY REGISTERED AS TYCO HEALTHCA |
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