FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VV330 Continuous ECG Platform, VivaLNK Adhesive Patch
K Number: K191870
·
Decision Jan 7, 2020
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
188
Applicant Total
1
Review Days
179
Basic Information
- Device Name
- VV330 Continuous ECG Platform, VivaLNK Adhesive Patch
- K Number
- K191870
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2910
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- VivaLNK, Inc.
- Date Received
- July 12, 2019
- Decision Date
- January 7, 2020
- Product Code
- DRG
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DRG | Transmitters And Receivers, Physiological Signal, Radiofrequency | FDA class 2 | Cardiovascular |
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