Medical Device Manufacturer · US , Newberg , OR

Inovise Medical, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2000

Recent clearances: AUDICOR CA300/CC100 Analyzer with SDB, AUDICOR CPAM WITH SDB (ACCELEROMETER BASED), AUDICOR CPAM WITH SDB (SINGLE SENSOR)

14
Total
14
Cleared
0
Denied

Inovise Medical, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Newberg, US.

Historical record: 14 cleared submissions from 2000 to 2016.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Inovise Medical, Inc.

14 devices
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