GWI — Discriminator, Two-Point Class I
FDA Device Classification
Classification Details
- Product Code
- GWI
- Device Class
- Class I
- Regulation Number
- 882.1200
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K944234 | jcm management and planning | TCD OR TCD NEUROPATHY STAR | March 8, 1995 |
| K874300 | orthopedic systems | AESTHESIOMETER | November 6, 1987 |