Device details
FDA 510(k) registration fields
- K number
- K170734
- Device name
- Venus Silk.expert
- Company
- Cyden Limited
- Country / region
- United Kingdom(GB)
- Product code
- GEX
- Device class
- Class 2
- Regulation number
- 21 CFR 878.4810
- Date received
- 2017-03-10
- Decision date
- 2017-05-08
- Submission type
- Special
- Technology type
- Other(AI inferred)
- Clinical applications
- Surgical cutting
- Primary application
- Surgical cutting
- Classification source
- AI classified