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FDA 510(k), K120518, END TIDAL CO2 NASAL CANNULA
FDA 510(k), K120518, END TIDAL CO2 NASAL CANNULA
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510(K) Number: K120518
Device Name: END TIDAL CO2 NASAL CANNULA
Manufacturer: CAREFUSION
Device Classification Name: analyzer, gas, carbon-dioxide, gaseous-phase
Regulation Number: 868.1400
Classification Product Code: CCK
Date Received: 02/21/2012
Decision Date: 05/04/2012
Regulation Medical Specialty: Anesthesiology
Device Name: END TIDAL CO2 NASAL CANNULA
Manufacturer: CAREFUSION
Device Classification Name: analyzer, gas, carbon-dioxide, gaseous-phase
Regulation Number: 868.1400
Classification Product Code: CCK
Date Received: 02/21/2012
Decision Date: 05/04/2012
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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