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FDA 510(k), K102757, LIFENET SYSTEM
FDA 510(k), K102757, LIFENET SYSTEM
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510(K) Number: K102757
Device Name: LIFENET SYSTEM
Manufacturer: PHYSIO-CONTROL, INC.
Device Classification Name: system, network and communication, physiological monitors
Regulation Number: 870.2300
Classification Product Code: MSX
Date Received: 09/23/2010
Decision Date: 11/05/2010
Regulation Medical Specialty: Cardiovascular
Device Name: LIFENET SYSTEM
Manufacturer: PHYSIO-CONTROL, INC.
Device Classification Name: system, network and communication, physiological monitors
Regulation Number: 870.2300
Classification Product Code: MSX
Date Received: 09/23/2010
Decision Date: 11/05/2010
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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