HOG — Burr, Corneal, Battery-Powered Class I
FDA product code HOG covers "Burr, Corneal, Battery-Powered", a Class I medical device regulated under 21 CFR 886.4070. Submissions are reviewed by the Ophthalmic panel. At least 5 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- HOG
- Device Class
- Class I
- Regulation Number
- 886.4070
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K962989 | s. percy amoils | AMOILS EPITHELIAL SCRUBBER | January 9, 1997 |
| K960261 | alcon laboratories | PALLIKARIS BRUSH | March 11, 1996 |
| K950520 | aaron medical industries | BURR, CORNEAL, BATTERY-POWERED | May 2, 1995 |
| K883785 | gy-ro industry | GY-RO SAFE | January 5, 1989 |
| K834354 | jedmed instrument | OPHTEC RUST RING REMOVER | March 19, 1984 |