UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET - Model 110.330

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

510(k) Number

K091154 ↗

FDA Product Code

JAQ

Models / Variants

110.270

Interstitial Ring Ct

Mr Applicator Set

Model 110.330

Device Class

Class II

Regulation

21 CFR Part 892.5700

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

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