Cleared Traditional

ANESTHESIA CONDUCTION FILTER

K902666 · Arbor Technologies, Inc. · Anesthesiology
Apr 1991
Decision
309d
Days
Class 2
Risk

About This 510(k) Submission

K902666 is an FDA 510(k) clearance for the ANESTHESIA CONDUCTION FILTER, a Filter, Conduction, Anesthetic (Class II — Special Controls, product code BSN), submitted by Arbor Technologies, Inc. (Ann Arbor, US). The FDA issued a Cleared decision on April 23, 1991, 309 days after receiving the submission on June 18, 1990. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.5130.

Submission Details

510(k) Number K902666 FDA.gov
FDA Decision Cleared SESE
Date Received June 18, 1990
Decision Date April 23, 1991
Days to Decision 309 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary —

Device Classification

Product Code BSN — Filter, Conduction, Anesthetic
Device Class Class II — Special Controls
CFR Regulation 21 CFR 868.5130

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