Ortho-Toluidine Reagent Set

by Fisher Scientific Co., LLC 510(k)

Active United States

510(k) K790319

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK790319	Date21 Mar 1979Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 11 Oct 2026.

Specification

510(k)

510(k) Number: K790319
FDA Product Code: CGE

Device Class: Class II
Regulation: 21 CFR Part 862.1345
Advisory Committee: Clinical Chemistry
FDA Decision: SESE Substantially Equivalent

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