Sonarmed, Inc.
FDA 510(k) medical device clearances, first cleared 2010, most recent 2020, with 5 FDA device recalls on record.
Top product codes for Sonarmed, Inc.
FDA recalls by Sonarmed, Inc.
- Z-1535-2024 — AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic Sensors for airway monitoring.
- Z-1519-2024 — AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
- Z-1520-2024 — AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed Monitor for airway monitoring.
- Z-1521-2024 — AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
- Z-2450-2019 — SonarMed AirWave Monitor, Model Number M0001
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Sonarmed, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.