FDA 510(k) Applications Submitted by INTERCURE LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020399 | 02/06/2002 | RESPERATE; MODEL RR-150 | INTERCURE LTD. |
| K000405 | 02/07/2000 | INTERCURE LTD. RESPI-LOW | INTERCURE LTD. |
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