Cleared Traditional

VANGUARD SERIES GAS REGULATORS

K942751 · Buckman Co., Inc. · Anesthesiology
Feb 1995
Decision
244d
Days
Class 1
Risk

About This 510(k) Submission

K942751 is an FDA 510(k) clearance for the VANGUARD SERIES GAS REGULATORS, a Regulator, Pressure, Gas Cylinder (Class I — General Controls, product code CAN), submitted by Buckman Co., Inc. (Concord, US). The FDA issued a Cleared decision on February 9, 1995, 244 days after receiving the submission on June 10, 1994. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.2700.

Submission Details

510(k) Number K942751 FDA.gov
FDA Decision Cleared SESE
Date Received June 10, 1994
Decision Date February 09, 1995
Days to Decision 244 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF

Device Classification

Product Code CAN — Regulator, Pressure, Gas Cylinder
Device Class Class I — General Controls
CFR Regulation 21 CFR 868.2700

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