Sinus Dilation System with Cannulated Instrument

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K131709 ↗

FDA Product Code

LRC

Device Class

Class I

Regulation

21 CFR Part 874.4420

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

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See all devices from ArthroCare Corporation →