510(k) K172801
K172801 is an FDA 510(k) premarket notification submitted by Cardiomedix, Inc. for the device "ECG SENTINEL System". The FDA issued a decision of Substantially Equivalent on Oct 18, 2017. The device falls under product code DXH (Transmitters And Receivers, Electrocardiograph, Telephone), a Class II device regulated under 21 CFR 870.2920.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 18, 2017
- Date Received
- Sep 18, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Transmitters And Receivers, Electrocardiograph, Telephone
- Device Class
- Class II
- Regulation Number
- 870.2920
- Review Panel
- CV
- Submission Type
- 510(k)