VM PLUS PEAK FLOWMETER— 510(k) K962074

Name: FDA 510(k) clearance K962074
Creator: U.S. Food and Drug Administration
Published: 1997-01-02

Substantially Equivalent

Clement Clarke Intl., Ltd.

FDA 510(k) clearance K962074 for VM PLUS PEAK FLOWMETER, Substantially Equivalent on 1997-01-02. Applicant: Clement Clarke Intl., Ltd.. Device class: 2.

Clearance details

Applicant: Clement Clarke Intl., Ltd.
Product code: Code BZH
Device class: Class 2
Regulation: 21 CFR 868.1860
Advisory panel: Anesthesiology
Date received: 1996-05-28
Decision date: 1997-01-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Harlow, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.