FDA 510(k) Applications for Medical Device Product Code "NPF"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K032403 | RESPIRONICS, INC. | SMARTMONITOR 2 PROFESSIONAL SERIES (PS) | 10/27/2003 |
K061256 | RESPIRONICS, INC. | SMARTMONITOR 2PS | 08/02/2006 |