Quicktox Multiple Drug Dipcard

by Branan Medical Corp. 510(k)

Active United States

510(k) K023489

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK023489	Date16 Dec 2002Cleared	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Withdrawn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 22 Oct 2026.

Specification

510(k)

510(k) Number: K023489
FDA Product Code: DIO

Device Class: Class II
Regulation: 21 CFR Part 862.3250
Advisory Committee: Clinical Toxicology
FDA Decision: SESE Substantially Equivalent

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