Feb Test

by Wako Chemicals USA, Inc. 510(k)

Active United States

510(k) K830564

Regulatory status

as of 26 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK830564	Date29 Mar 1983Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 9 Oct 2026)

Specification

510(k)

510(k) Number: K830564
FDA Product Code: CFM

Device Class: Class I
Regulation: 21 CFR Part 862.1410
Advisory Committee: Clinical Chemistry
FDA Decision: SESE Substantially Equivalent

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