Model 795 Fluorometer/Densitometer

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

510(k) Number

K915332 ↗

FDA Product Code

JQT

Device Class

Class I

Regulation

21 CFR Part 862.2400

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

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See all devices from Ciba Corning Diagnostics Corp. →