Fever Scout
510(k) K181013
Fever Scout is a Class II device made by VivaLNK, Inc., cleared under FDA 510(k) K181013 on 21 Aug 2018, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK181013 | Date21 Aug 2018 | StatusActive |
Official records
- FDA 510(k) database K181013
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- FLL
- Device class
- Class II
- Regulation
- 21 CFR Part 880.2910
- Advisory committee
- General Hospital
- FDA decision
- SESE Substantially Equivalent
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