← FDA Medical Device Classifications
Cranial Electrotherapy Stimulator To Treat Depression
JXK · Class III — High Risk (PMA approval required, life-sustaining) · Neurology · 21 CFR 882.5800
Classification
- FDA Product Code
JXK- Device class
- Class III — High Risk (PMA approval required, life-sustaining)
- Regulation
- 21 CFR 882.5800
- Review panel
- NE
- Medical specialty
- Neurology
- Submission type
- 2
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 3
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown