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FDA 510(k), K090671, PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D
FDA 510(k), K090671, PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D
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510(K) Number: K090671
Device Name: PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D
Manufacturer: CONTEC MEDICAL SYSTEM CO., LTD.
Device Classification Name: oximeter
Regulation Number: 870.2700
Classification Product Code: DQA
Date Received: 03/13/2009
Decision Date: 06/11/2009
Regulation Medical Specialty: Cardiovascular
Device Name: PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D
Manufacturer: CONTEC MEDICAL SYSTEM CO., LTD.
Device Classification Name: oximeter
Regulation Number: 870.2700
Classification Product Code: DQA
Date Received: 03/13/2009
Decision Date: 06/11/2009
Regulation Medical Specialty: Cardiovascular
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- Delivery: Approximately 1 to 2 weeks
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