LZPClass III
Aid, Surgical, Viscoelastic
21 CFR 886.4275 / Ophthalmic
LZP is the FDA product code for Aid, Surgical, Viscoelastic, a class III device type, regulated under 21 CFR 886.4275. As of , FDA records hold no 510(k) clearances under this code and 25 recalls.
Classification record
- Product code
- LZP
- Device name
- Aid, Surgical, Viscoelastic
- Regulation
- 21 CFR 886.4275
- Device class
- Class III
- Review panel
- Ophthalmic
- Submission type
- PMA
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 0
- Ingested recalls
- 25
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
