GWI
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Discriminator, Two-Point
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 882.1200
- Medical specialty
- Neurology
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| TCD OR TCD NEUROPATHY STAR (K944234) | Jcm Management & Planning Co. | 1995-03-08 |
| AESTHESIOMETER (K874300) | Orthopedic Systems, Inc. | 1987-11-06 |
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Every clearance here is in the API, with alerts when new ones post.