FDA 510(k) Applications Submitted by RIMED LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062578 | 08/31/2006 | DIGI-LITE TCD DEVICE | RIMED LTD. |
| K143476 | 12/05/2014 | Digi-One | RIMED LTD. |
| K974588 | 12/09/1997 | INTRA-VIEW BILATERAL TRANSCRANIAL DOPPLER DEVICE, SMART-LITE PORTABLE BILATERAL TRANSCRANIAL DOPPLER DEVICE, COMPACT MOD | RIMED LTD. |
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