Cleared Traditional

K042838 - VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 23 (FDA 510(k) Clearance)

Also includes:
VITROS CHEMISTRY PRODUCTS PALB PERFORMANCE VERIFIERS I & II
Dec 2004
Decision
56d
Days
Class 2
Risk

K042838 is an FDA 510(k) clearance for the VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 23. This device is classified as a Calibrator, Secondary (Class II - Special Controls, product code JIT).

Submitted by Ortho-Clinical Diagnostics, Inc. (Rochester, US). The FDA issued a Cleared decision on December 9, 2004, 56 days after receiving the submission on October 14, 2004.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1150.

Submission Details

510(k) Number K042838 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 14, 2004
Decision Date December 09, 2004
Days to Decision 56 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code JIT — Calibrator, Secondary
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1150