Ultralith Ultrasonic Lithotripsy System

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K850298 ↗

FDA Product Code

FEO

Device Class

Class II

Regulation

21 CFR Part 876.4480

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

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See all devices from Cabot Medical Corp. →