Product code HMC— Ophthalmic
ORTHOMET LHMC FEMORAL STEM
- Classification name
- Monitor, Eye Movement, Diagnostic
- Device class
- Class 2
- Regulation
- 21 CFR 886.1510
- Advisory panel
- Ophthalmic
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code HMC
FDA has cleared device under product code HMC, all in 1994, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Top applicants under product code HMC
Recent clearances under product code HMC
Data sourced from openFDA. This site is unofficial and independent of the FDA.