510(k) K183369
K183369 is an FDA 510(k) premarket notification submitted by Corscience GmbH & Co. for the device "COR12 ECG". The FDA issued a decision of Substantially Equivalent on Dec 28, 2018. 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
- Dec 28, 2018
- Date Received
- Dec 4, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Electrocardiograph
- Device Class
- Class II
- Regulation Number
- 870.2340
- Review Panel
- CV
- Submission Type
- 510(k)