510(k) K170154
K170154 is an FDA 510(k) premarket notification submitted by Creavo Medical Technologies, Ltd. for the device "Creavo Vitalscan Magnetocardiograph". The FDA issued a decision of Substantially Equivalent on Oct 12, 2017. The device falls under product code DPS (Electrocardiograph), a Class II device regulated under 21 CFR 870.2340.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 12, 2017
- Date Received
- Jan 18, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrocardiograph
- Device Class
- Class II
- Regulation Number
- 870.2340
- Review Panel
- CV
- Submission Type
- 510(k)