IQTEQ SPIROMETER— 510(k) K020102

Substantially Equivalent

Iqteq Development

FDA 510(k) clearance K020102 for IQTEQ SPIROMETER, Substantially Equivalent on 2003-03-21. Applicant: Iqteq Development. Device class: 2.

Clearance details

Applicant: Iqteq Development
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 2002-01-11
Decision date: 2003-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cape Town, Western Cape, ZA

Download summary PDF View on FDA.gov ↗

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