FDA 510(k) Applications for Medical Device Product Code "NMD"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K100523 | HYGIA HEALTH SERVICES, INC. | ADULT CEREBRAL-SOMATIC OXIMETRY SENSOR, PEDIATRIC CEREBRAL-SOMATIC OXIMETRY SENSOR MODEL HHS-SAFB-SM, HHS-SPFB-USA | 05/04/2010 |
K111007 | MIDWEST REPROCESSING CENTER LLC | MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE | 06/08/2011 |