Product code HMD— Ophthalmic
DOWING OPHTHALMIC CHAIR-NON/AC POWER
- Classification name
- Chair, Ophthalmic, Manual
- Device class
- Class 1
- Regulation
- 21 CFR 886.1140
- Advisory panel
- Ophthalmic
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code HMD
FDA has cleared device under product code HMD, all in 1984, filed by 1 applicant company. 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.
Top applicants under product code HMD
Recent clearances under product code HMD
Data sourced from openFDA. This site is unofficial and independent of the FDA.