510(k) K200026
K200026 is an FDA 510(k) premarket notification submitted by Shenzhen Changke Connect Electronics Co., Ltd. for the device "Disposable ECG Cable". The FDA issued a decision of Substantially Equivalent on May 12, 2020. The device falls under product code DSA (Cable, Transducer And Electrode, Patient, (Including Connector)), a Class II device regulated under 21 CFR 870.2900. Shenzhen Changke Connect Electronics Co., Ltd. has 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 12, 2020
- Date Received
- Jan 6, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cable, Transducer And Electrode, Patient, (Including Connector)
- Device Class
- Class II
- Regulation Number
- 870.2900
- Review Panel
- CV
- Submission Type
- 510(k)