Cleared Traditional

K961161 - AVL OPTI 1 PH/BLOOD GAS ANALYZER
(FDA 510(k) Clearance)

Apr 1996
Decision
35d
Days
Class 2
Risk

K961161 is an FDA 510(k) clearance for the AVL OPTI 1 PH/BLOOD GAS 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 Avl Scientific Corp. (Roswell, US). The FDA issued a Cleared decision on April 26, 1996, 35 days after receiving the submission on March 22, 1996.

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

Submission Details

510(k) Number K961161 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 22, 1996
Decision Date April 26, 1996
Days to Decision 35 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

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