Cleared Traditional

K990531 - VITROS IMMUNODIAGNOSTIC PRODUCTS ONCOLOGY CONTROLS (FDA 510(k) Clearance)

Mar 1999
Decision
21d
Days
Class 1
Risk

K990531 is an FDA 510(k) clearance for the VITROS IMMUNODIAGNOSTIC PRODUCTS ONCOLOGY CONTROLS. This device is classified as a Multi-analyte Controls, All Kinds (assayed) (Class I - General Controls, product code JJY).

Submitted by Ortho-Clinical Diagnostics, Inc. (Rochester, US). The FDA issued a Cleared decision on March 12, 1999, 21 days after receiving the submission on February 19, 1999.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1660.

Submission Details

510(k) Number K990531 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 19, 1999
Decision Date March 12, 1999
Days to Decision 21 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code JJY — Multi-analyte Controls, All Kinds (assayed)
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.1660