Inovise Medical, Inc.
Inovise Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2016.
Top product codes for Inovise Medical, Inc.
Recent clearances by Inovise Medical, Inc.
- K151433 — AUDICOR CA300/CC100 Analyzer with SDB
- K131883 — AUDICOR CPAM WITH SDB (ACCELEROMETER BASED)
- K130660 — AUDICOR CPAM WITH SDB (SINGLE SENSOR)
- K120462 — AUDICOR CPAM WITH SDB (CARDIOPULMONARY AMBULATORY MONITOR WITH SLEEP DISORDERED BREATHING DETECTION)
- K110569 — AUDICOR CPAM (CARDIOPULMONARY AMBULATORY MONITOR)
- K103516 — AUDICOR SENSOR-ADAPTER MODEL AUDICOR SENSOR-ADAPTER 4.0
- K080602 — AUDICOR SENSOR, MODELS: 2.0, 3.0
- K073545 — AUDICOR, HEMO AMBULATORY MONITOR
- K070136 — AUDICOR 200 SYSTEM, MODELS 200D AND 200S
- K051450 — EXTENDED MEASUREMENTS SYSTEM
- K043074 — LIBERTY SYSTEM
- K032145 — AUDICOR UPGRADE SYSTEM
- K030316 — AUDICOR COR SENSOR (AND ACCESSORY ADAPTOR)
- K001349 — CARDIOVISE ECG INTERPRETATIVE SOFTWARE
Data sourced from openFDA. This site is unofficial and independent of the FDA.