DeviceClearance

Product code FFS— Gastroenterology, Urology

FIBER OPTIC ENDOILLUMINATION PROBE

Classification name
Image, Illumination, Fiberoptic, For Endoscope
Device class
Class 2
Regulation
21 CFR 876.1500
Advisory panel
Gastroenterology, Urology
Total cleared
26
First cleared
Most recent

Market context for product code FFS

FDA has cleared 26 devices under product code FFS between 1984 and 2007, filed by 22 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

Top applicants under product code FFS

Recent clearances under product code FFS

Data sourced from openFDA. This site is unofficial and independent of the FDA.