Product code LYH— Physical Medicine

FDA has cleared 5 devices under product code LYH between 1981 and 1995, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19951 clearance
• 19941 clearance
• 19881 clearance
• 19841 clearance
• 19811 clearance

• Medmetric Corp.3 clearances
• Far Orthopedics, Inc.1 clearance
• Dyonics, Inc.1 clearance

• K943197 — KT1000/S KNEE LIGAMENT ARTHROMETERMedmetric Corp.·1995-03-02
• K942059 — KT2000 KNEE LIGAMENT ARTHROMETERMedmetric Corp.·1994-09-20
• K881876 — DYNAMIC CRUCIATE TESTERDyonics, Inc.·1988-11-17
• K834462 — GENUCOMFar Orthopedics, Inc.·1984-02-09
• K812806 — KT-1000 DEVICEMedmetric Corp.·1981-11-10