PUL
- Product code
- PUL
- Device name
- Apparatus, Cutting, Radiofrequency, Electrosurgical, Ac-Powered
- Device class
- Class 2
- 21 CFR
- 21 CFR 886.4100
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 4 (all years; only the last 3 years are listed here)
FDA classification definition
Used to perform anterior capsulotomy during cataract surgery
Official FDA classification page: PUL
Classification and pathway per current FDA publications. Data from openFDA (CC0).