Dial X Collimator Model a&B

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K771689 ↗

FDA Product Code

IZX

Device Class

Class II

Regulation

21 CFR Part 892.1610

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

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See all devices from Bennett X-Ray Corp. →