Cleared Traditional

K935069 - IL1430 BGELECTROLYTE ANALYZER (FDA 510(k) Clearance)

Mar 1994
Decision
154d
Days
Class 2
Risk

K935069 is an FDA 510(k) clearance for the IL1430 BGELECTROLYTE ANALYZER. This device is classified as a Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph (Class II - Special Controls, product code CHL).

Submitted by Instrumentation Laboratory CO (Bedford, US). The FDA issued a Cleared decision on March 28, 1994, 154 days after receiving the submission on October 25, 1993.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1120.

Submission Details

510(k) Number K935069 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 25, 1993
Decision Date March 28, 1994
Days to Decision 154 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code CHL — Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1120