RESPIRATION MONITOR 1000— 510(k) K820778

Name: FDA 510(k) clearance K820778
Creator: U.S. Food and Drug Administration
Published: 1982-05-03

Substantially Equivalent

Intl. Medical Devices , Ltd.

FDA 510(k) clearance K820778 for RESPIRATION MONITOR 1000, Substantially Equivalent on 1982-05-03. Applicant: Intl. Medical Devices , Ltd.. Device class: 2.

Clearance details

Applicant: Intl. Medical Devices , Ltd.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1982-03-23
Decision date: 1982-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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