Neurosign V4 Intraoperative Nerve Monitor— 510(k) K203684
Substantially EquivalentMagstim Company, Ltd.
FDA 510(k) clearance K203684 for Neurosign V4 Intraoperative Nerve Monitor, Substantially Equivalent on 2021-03-17. Applicant: Magstim Company, Ltd.. Device class: 2.
Clearance details
- Applicant
- Magstim Company, Ltd.
- Product code
- Code PDQ
- Device class
- Class 2
- Regulation
- 21 CFR 874.1820
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Whitland, GB
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More clearances from Magstim Company, Ltd.
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- K183376 — HORIZON TMS Therapy System with Navigation
- K182853 — HORIZON TMS Therapy System
Data sourced from openFDA. This site is unofficial and independent of the FDA.