KZN
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Scanner, Color
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 872.3661
- Medical specialty
- Dental
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US (K072643) | Olympus Corporation | 2007-11-16 |
| CHROMASCAN TM (K770667) | Sterndent Corp. | 1977-04-20 |
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Every clearance here is in the API, with alerts when new ones post.