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FDA 510(k)

CAIRD TECHNOLOGY SPIROMETER

K-Number: K971336 · 1998-12-01

ApplicantCaird Technology
Decision Date1998-12-01
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAIRD TECHNOLOGY SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Caird Technology. It received FDA 510(k) clearance on 1998-12-01 under 510(k) number K971336. 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 CAIRD TECHNOLOGY SPIROMETER?

CAIRD TECHNOLOGY SPIROMETER is a medical device that received FDA 510(k) clearance on 1998-12-01. The listed applicant is Caird Technology. The 510(k) number is K971336.

When did CAIRD TECHNOLOGY SPIROMETER receive FDA 510(k) clearance?

CAIRD TECHNOLOGY SPIROMETER received FDA 510(k) clearance on 1998-12-01, under 510(k) number K971336.

Who is the listed applicant for CAIRD TECHNOLOGY SPIROMETER?

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

What is the FDA product code for CAIRD TECHNOLOGY SPIROMETER?

The FDA product code for CAIRD TECHNOLOGY SPIROMETER is BZG.

Related Clinical Trials

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.

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Other records listing Caird Technology as applicant

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.

K101016ANS SYSTEMK012686CAIRD TECHNOLOGY HOLTER 2000

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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