Cleared Traditional

AIRCO PRESSURE REGULATORS

K862796 · Airco, Inc. · Anesthesiology

Aug 1986

Decision

17d

Days

Class 1

Risk

About This 510(k) Submission

K862796 is an FDA 510(k) clearance for the AIRCO PRESSURE REGULATORS, a Regulator, Pressure, Gas Cylinder (Class I — General Controls, product code CAN), submitted by Airco, Inc. (Virginia Beach, US). The FDA issued a Cleared decision on August 8, 1986, 17 days after receiving the submission on July 22, 1986. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.2700.

Submission Details

510(k) Number	K862796 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 22, 1986
Decision Date	August 08, 1986
Days to Decision	17 days
Submission Type	Traditional
Review Panel	Anesthesiology (AN)
Summary	—