Product code NCF— Ophthalmic
ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM
- Classification name
- Aberrometer, Ophthalmic
- Device class
- Class 1
- Regulation
- 21 CFR 886.1760
- Advisory panel
- Ophthalmic
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code NCF
FDA has cleared devices under product code NCF between 2000 and 2006, 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.
Clearances per year
- 2006
- 2005
- 2002
- 2000
Top applicants under product code NCF
Adverse events under product code NCF
product code NCF- Injury
- 129
- Total
- 129
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code NCF
Data sourced from openFDA. This site is unofficial and independent of the FDA.