LYH
5 FDA 510(k) clearances · Product code
144 daysmedian time to decision
240 days90th percentile
5clearances measured
FDA profile
- Official device name
- Arthrometer
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.1615
- Medical specialty
- Physical Medicine
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| KT1000/S KNEE LIGAMENT ARTHROMETER (K943197) | Medmetric Corp. | 1995-03-02 |
| KT2000 KNEE LIGAMENT ARTHROMETER (K942059) | Medmetric Corp. | 1994-09-20 |
| DYNAMIC CRUCIATE TESTER (K881876) | Dyonics, Inc. | 1988-11-17 |
| GENUCOM (K834462) | Far Orthopedics, Inc. | 1984-02-09 |
| KT-1000 DEVICE (K812806) | Medmetric Corp. | 1981-11-10 |
Track LYH automatically
Every clearance here is in the API, with alerts when new ones post.