Cleared Traditional

K150955 - Elecsys Progesterone III Cal Check 5 (FDA 510(k) Clearance)

May 2015
Decision
22d
Days
Class 1
Risk

K150955 is an FDA 510(k) clearance for the Elecsys Progesterone III Cal Check 5. This device is classified as a Single (specified) Analyte Controls (assayed And Unassayed) (Class I - General Controls, product code JJX).

Submitted by Roche Diagnostics (Indianapolis, US). The FDA issued a Cleared decision on May 1, 2015, 22 days after receiving the submission on April 9, 2015.

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

Submission Details

510(k) Number K150955 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 09, 2015
Decision Date May 01, 2015
Days to Decision 22 days
Submission Type Traditional
Review Panel Chemistry (CH)
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