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.

Clearance details

Applicant: Iqteq Development
Product code: Code BZG
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

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