Product code DQF— Cardiovascular
ALCON FLUID INJECTOR
- Classification name
- Actuator, Syringe, Injector Type
- Device class
- Class 2
- Regulation
- 21 CFR 870.1670
- Advisory panel
- Cardiovascular
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code DQF
FDA has cleared devices under product code DQF between 1988 and 1992, filed by 3 applicant companies. 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.
Clearances per year
- 1992
- 1988
Top applicants under product code DQF
Recent clearances under product code DQF
Data sourced from openFDA. This site is unofficial and independent of the FDA.