Product code FTZ— Ophthalmic
MODEL 200
- Classification name
- Locator, Magnetic
- Device class
- Class 1
- Regulation
- 21 CFR 886.4445
- Advisory panel
- Ophthalmic
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code FTZ
FDA has cleared devices under product code FTZ between 1983 and 1984, filed by 2 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.
Clearances per year
- 1984
- 1983
Top applicants under product code FTZ
Recent clearances under product code FTZ
Data sourced from openFDA. This site is unofficial and independent of the FDA.