Cleared Traditional

K212576 - MDx-Chex for BCID2 (FDA 510(k) Clearance)

Jan 2022
Decision
156d
Days
Class 2
Risk

K212576 is an FDA 510(k) clearance for the MDx-Chex for BCID2. This device is classified as a Assayed External Control Material For Microbiology Nucleic Acid Amplification (nat) Assays (Class II - Special Controls, product code PMN).

Submitted by Streck, Inc. (La Vista, US). The FDA issued a Cleared decision on January 19, 2022, 156 days after receiving the submission on August 16, 2021.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3920. Assayed External Quality Control Material To Monitor The Performance Of Microbiology Nucleic Acid Assays For In Vitro Diagnostic Use..

Submission Details

510(k) Number K212576 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 16, 2021
Decision Date January 19, 2022
Days to Decision 156 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF

Device Classification

Product Code PMN - Assayed External Control Material For Microbiology Nucleic Acid Amplification (nat) Assays
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.3920
Definition Assayed External Quality Control Material To Monitor The Performance Of Microbiology Nucleic Acid Assays For In Vitro Diagnostic Use.