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Vitros Chemistry Products Cocm Reagent, Calibrator Kit 26, Fs Calibrator 1 and Dat Performance Verifiers I, II, III, IV

by Ortho-Clinical Diagnostics, Inc.

510(k) K062123

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK062123 Date16 Nov 2006ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0817-2014 FDA Class II initiated 4 Oct 2013

    Inaccurate quality control results.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
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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