Gentamicin Fluroimmunassay Kit

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K782025 ↗

FDA Product Code

LCQ

FDA applicant

Technia Diagnostics , Ltd.

Device Class

Class II

Regulation

21 CFR Part 862.3450

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

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• T3(125) Radioimmunoassay Kit

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See all devices from Technia Diagnostics, Ltd. →