HMS — Drum, Eye Knife Test Class I
FDA product code HMS covers "Drum, Eye Knife Test", a Class I medical device regulated under 21 CFR 886.4230. 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
- HMS
- Device Class
- Class I
- Regulation Number
- 886.4230
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K926412 | chiron vision | MICRON-SCOPE II | July 19, 1994 |