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FDA 510(k), K111773, RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
FDA 510(k), K111773, RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
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510(K) Number: K111773
Device Name: RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
Manufacturer:
Device Classification Name: Oximeter, Reprocessed
Regulation Number: 870.2700
Classification Product Code: NLF
Date Received: 06/23/2011
Decision Date: 11/16/2011
Regulation Medical Specialty: Cardiovascular
Device Name: RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
Manufacturer:
Device Classification Name: Oximeter, Reprocessed
Regulation Number: 870.2700
Classification Product Code: NLF
Date Received: 06/23/2011
Decision Date: 11/16/2011
Regulation Medical Specialty: Cardiovascular
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