V-Patch Cardiac Monitor— 510(k) K222842
Substantially EquivalentShandong Corecare Technology Limited
FDA 510(k) clearance K222842 for V-Patch Cardiac Monitor, Substantially Equivalent on 2022-10-20. Applicant: Shandong Corecare Technology Limited. Device class: 2.
Clearance details
- Applicant
- Shandong Corecare Technology Limited
- Product code
- Code DXH
- Device class
- Class 2
- Regulation
- 21 CFR 870.2920
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jinan, CN
Recent devices under product code DXH
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