HJA
5 FDA 510(k) clearances · Product code
70 daysmedian time to decision
101 days90th percentile
5clearances measured
FDA profile
- Official device name
- Photokeratoscope
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1350
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| VKG 1000, VIDEO KERATOGRAPH (K901523) | The Sanborn Co. | 1990-06-27 |
| VKG 2000 VIDEO KERATOMETER (K893968) | Technitex, Inc. | 1989-09-11 |
| AMERICAN MEDICAL OPTICS PHOTOKERATO (K842128) | American Medical Optics | 1984-08-07 |
| DORC CONTACT/PHOTO DERATOSCOPE (K830290) | Jedmed Instrument Co. | 1983-03-09 |
| TERRY KERATOMETER (K781650) | Clifford M. Terry, M.C. | 1978-10-17 |
Track HJA automatically
Every clearance here is in the API, with alerts when new ones post.