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FDA 510(k), K141877, LEAF PATIENT MONITORING SYSTEM
FDA 510(k), K141877, LEAF PATIENT MONITORING SYSTEM
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510(K) Number: K141877
Device Name: LEAF PATIENT MONITORING SYSTEM
Manufacturer: LEAF HEALTHCARE, INC.
Device Classification Name: Monitor, Bed Patient
Regulation Number: 880.2400
Classification Product Code: KMI
Date Received: 07/11/2014
Decision Date: 11/10/2014
Regulation Medical Specialty: General Hospital
Device Name: LEAF PATIENT MONITORING SYSTEM
Manufacturer: LEAF HEALTHCARE, INC.
Device Classification Name: Monitor, Bed Patient
Regulation Number: 880.2400
Classification Product Code: KMI
Date Received: 07/11/2014
Decision Date: 11/10/2014
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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