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FDA 510(k), K030952, DOLPHIN 2000 PULSE OXIMETRY SENSORS MODELS 2010, 2311 ADULT, 2312 PEDIATRIC, 2313 INFANT, 2314 NEONATAL, 2421
FDA 510(k), K030952, DOLPHIN 2000 PULSE OXIMETRY SENSORS MODELS 2010, 2311 ADULT, 2312 PEDIATRIC, 2313 INFANT, 2314 NEONATAL, 2421
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510(K) Number: K030952
Device Name: DOLPHIN 2000 PULSE OXIMETRY SENSORS MODELS 2010, 2311 ADULT, 2312 PEDIATRIC, 2313 INFANT, 2314 NEONATAL, 2421
Manufacturer: BILL CURNAN
Device Classification Name: Oximeter
Regulation Number: DQA
Classification Product Code: 03/26/2003
Date Received: 05/19/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: DOLPHIN 2000 PULSE OXIMETRY SENSORS MODELS 2010, 2311 ADULT, 2312 PEDIATRIC, 2313 INFANT, 2314 NEONATAL, 2421
Manufacturer: BILL CURNAN
Device Classification Name: Oximeter
Regulation Number: DQA
Classification Product Code: 03/26/2003
Date Received: 05/19/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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