← FDA Medical Device Classifications
Non-Invasive Vagus Nerve Stimulator For Migraine Headache
QAK · Class II — Moderate Risk (510(k) clearance required) · Neurology · 21 CFR 882.5892
Classification
- FDA Product Code
QAK- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 882.5892
- Review panel
- NE
- Medical specialty
- Neurology
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Definition
The device intended for non-invasive vagus nerve stimulation (nVNS) on the side of the neck to treat migraine headache.
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 1
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown