HLG
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Pupillometer, Ac-Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1700
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| COMPUTERIZED PUPIL (K920937) | Trek Medical Products, Inc. | 1992-10-02 |
| PUPIL PATHWAY ANALYZER (PPA) (K895609) | Pulse Medical Instruments | 1989-11-02 |
| F110 PHOTO BINOCULAR OPHTHALMOSCOPE (K802351) | Minami, Tomine & Lew | 1980-12-17 |
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Every clearance here is in the API, with alerts when new ones post.