Medical Device Manufacturer · US , Indianapolis , IN

Sonarmed, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2010

Recent clearances: SonarMed AirWave Airway Monitoring System, SonarMed AirWave, Airway Monitoring System, SONARMED AIRWAY MONITORING SYSTEM, MODEL 0901

View 3 510(k) Devices ↓
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Sonarmed, Inc. Anesthesiology ✕

3 devices
1-3 of 3
Cleared May 15, 2020
SonarMed AirWave Airway Monitoring System
K193058 · OQU
Anesthesiology · 196d
Cleared Jan 22, 2016
SonarMed AirWave, Airway Monitoring System
K143042 · OQU
Anesthesiology · 457d
Cleared Apr 28, 2010
SONARMED AIRWAY MONITORING SYSTEM, MODEL 0901
K092611 · OQU
Anesthesiology · 245d
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