Cleared Traditional

K152526 - Elecsys Progesterone III CalSet (FDA 510(k) Clearance)

Oct 2015
Decision
29d
Days
Class 2
Risk

K152526 is an FDA 510(k) clearance for the Elecsys Progesterone III CalSet. This device is classified as a Calibrator, Secondary (Class II - Special Controls, product code JIT).

Submitted by Roche Diagnostics (Indianapolis, US). The FDA issued a Cleared decision on October 2, 2015, 29 days after receiving the submission on September 3, 2015.

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

Submission Details

510(k) Number K152526 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 03, 2015
Decision Date October 02, 2015
Days to Decision 29 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