Natus VikingQuest
by Natus Neurology Incorporated
510(k) K172743
Natus VikingQuest is a Class II device made by Natus Neurology Incorporated, cleared under FDA 510(k) K172743 on 19 Dec 2017, 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 | NumberK172743 | Date19 Dec 2017 | StatusActive |
Official records
- FDA 510(k) database K172743
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IKN
- Device class
- Class II
- Regulation
- 21 CFR Part 890.1375
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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