Cleared Traditional

K033127 - VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC CONTROLS (FDA 510(k) Clearance)

Oct 2003
Decision
31d
Days
Class 1
Risk

K033127 is an FDA 510(k) clearance for the VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC CONTROLS. This device is classified as a Single (specified) Analyte Controls (assayed And Unassayed) (Class I - General Controls, product code JJX).

Submitted by Ortho-Clinical Diagnostics (Rochester, US). The FDA issued a Cleared decision on October 31, 2003, 31 days after receiving the submission on September 30, 2003.

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

Submission Details

510(k) Number K033127 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 2003
Decision Date October 31, 2003
Days to Decision 31 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF

Device Classification

Product Code JJX — Single (specified) Analyte Controls (assayed And Unassayed)
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.1660