HOW — Drum, Opticokinetic Class I
FDA product code HOW covers "Drum, Opticokinetic", a Class I medical device regulated under 21 CFR 886.1200. 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
- HOW
- Device Class
- Class I
- Regulation Number
- 886.1200
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K822917 | life-tech intl | MODEL 5400 OPTOKINETIC STIMULATOR | November 1, 1982 |