LWL — Fluid, Intraocular Class III
FDA product code LWL covers "Fluid, Intraocular", a Class III medical device regulated under 21 CFR 886.4275. Submissions are reviewed by the Ophthalmic panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LWL
- Device Class
- Class III
- Regulation Number
- 886.4275
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K844895 | optical micro systems | OMS SILICONE OIL INJECTOR | June 24, 1985 |