FDA 510(k) Applications Submitted by CRITISENSE LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062977 | 09/29/2006 | CRITIVIEW, MODEL CRV3 | CRITISENSE LTD. |
| K051145 | 05/04/2005 | CRITIVIEW | CRITISENSE LTD. |
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