Tobramycin Fpia Reagent Set and Calibrator

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K944371 ↗

FDA Product Code

LFW

Device Class

Class II

Regulation

21 CFR Part 862.3900

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

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See all devices from Sigma Diagnostics, Inc. →