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FDA 510(k)

IQTEQ SPIROMETER

K-Number: K020102 · 2003-03-21

ApplicantIqteq Development
Decision Date2003-03-21
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IQTEQ SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Iqteq Development. It received FDA 510(k) clearance on 2003-03-21 under 510(k) number K020102. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IQTEQ SPIROMETER?

IQTEQ SPIROMETER is a medical device that received FDA 510(k) clearance on 2003-03-21. The listed applicant is Iqteq Development. The 510(k) number is K020102.

When did IQTEQ SPIROMETER receive FDA 510(k) clearance?

IQTEQ SPIROMETER received FDA 510(k) clearance on 2003-03-21, under 510(k) number K020102.

Who is the listed applicant for IQTEQ SPIROMETER?

The FDA 510(k) record lists Iqteq Development as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IQTEQ SPIROMETER?

The FDA product code for IQTEQ SPIROMETER is BZG.

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Related Devices (Code: BZG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair ABK230501Spirobank OxiMir Medical International Research USAK230178EasyOne Sky SpirometerNdd Medizintechnik AGK222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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