NDD MEDICAL TECHNOLOGIES EASYONE SPIROMETER: FRONTLINE MODEL 2000 AND DIAGNOSTIC MODEL 2001— 510(k) K993921

Name: FDA 510(k) clearance K993921
Creator: U.S. Food and Drug Administration
Published: 2000-05-23

Substantially Equivalent

Ndd Medical Technologies

FDA 510(k) clearance K993921 for NDD MEDICAL TECHNOLOGIES EASYONE SPIROMETER: FRONTLINE MODEL 2000 AND DIAGNOSTIC MODEL 2001, Substantially Equivalent on 2000-05-23. Applicant: Ndd Medical Technologies. Device class: 2.

Clearance details

Applicant: Ndd Medical Technologies
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1999-11-18
Decision date: 2000-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chelmsford, MA, US

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