Cleared Traditional

K832251 - PRECISET CHOLESTEROL HIGH PERFORM (FDA 510(k) Clearance)

Aug 1983
Decision
44d
Days
Class 2
Risk

K832251 is an FDA 510(k) clearance for the PRECISET CHOLESTEROL HIGH PERFORM. This device is classified as a Calibrator, Primary (Class II - Special Controls, product code JIS).

Submitted by Boehringer Mannheim Corp. (Mchenry, US). The FDA issued a Cleared decision on August 24, 1983, 44 days after receiving the submission on July 11, 1983.

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

Submission Details

510(k) Number K832251 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 11, 1983
Decision Date August 24, 1983
Days to Decision 44 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code JIS — Calibrator, Primary
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1150