Ventrex Ip Specific E Enzyme Immunoassay

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

510(k) Number

K870624 ↗

FDA Product Code

DHB

Device Class

Class II

Regulation

21 CFR Part 866.5750

Advisory Committee

Immunology

FDA Decision

SESE Substantially Equivalent

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See all devices from Ventrex Laboratories, Inc. →