MYD — Keratome, Water Jet Class I
FDA product code MYD covers "Keratome, Water Jet", a Class I medical device regulated under 21 CFR 886.4370. 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
- MYD
- Device Class
- Class I
- Regulation Number
- 886.4370
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K991124 | visijet | VISIJET HYDROKERATOME, MODEL 50 | October 20, 2000 |