PULMOLAB EX671 EXERCISE TESTING SYSTEM— 510(k) K020280

Name: FDA 510(k) clearance K020280
Creator: U.S. Food and Drug Administration
Published: 2002-09-24

Substantially Equivalent

Morgan Medical , Ltd.

FDA 510(k) clearance K020280 for PULMOLAB EX671 EXERCISE TESTING SYSTEM, Substantially Equivalent on 2002-09-24. Applicant: Morgan Medical , Ltd.. Device class: 2.

Clearance details

Applicant: Morgan Medical , Ltd.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 2002-01-28
Decision date: 2002-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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