Ucd Urine Specimen Collector

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K854173 ↗

FDA Product Code

KNX

Device Class

Class II

Regulation

21 CFR Part 876.5250

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

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See all devices from Baker Instructions Corp. →