510(k) K113485
K113485 is an FDA 510(k) premarket notification submitted by Shenzhen Carewell Electronics Co., Ltd. for the device "ELECTROCARDIOGRAPH". The FDA issued a decision of Substantially Equivalent on Apr 25, 2012. The device falls under product code DPS (Electrocardiograph), a Class II device regulated under 21 CFR 870.2340. Shenzhen Carewell Electronics Co., Ltd. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 25, 2012
- Date Received
- Nov 23, 2011
- 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)