• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K150174, EMMA, by Inrange Systems, Inc.

FDA 510(k) K150174, EMMA, by Inrange Systems, Inc.

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510(K) Number: K150174
Device Name: EMMA
Manufacturer: Inrange Systems, Inc.
Device Classification Name: medication management system, remote
Regulation Number: 880.6315
Classification Product Code: NZH
Date Received: 01/26/2015
Decision Date: 02/26/2015
Regulation Medical Specialty: General Hospital

118 Pages (115 of 233 pages are fully redacted)
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