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FDA 510(k)

KOKO SPIROMETER

K-Number: K914272 · 1992-07-02

ApplicantFerraris Respiratory, Inc.
Decision Date1992-07-02
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KOKO SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Ferraris Respiratory, Inc.. It received FDA 510(k) clearance on 1992-07-02 under 510(k) number K914272. 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 KOKO SPIROMETER?

KOKO SPIROMETER is a medical device that received FDA 510(k) clearance on 1992-07-02. The listed applicant is Ferraris Respiratory, Inc.. The 510(k) number is K914272.

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

KOKO SPIROMETER received FDA 510(k) clearance on 1992-07-02, under 510(k) number K914272.

Who is the listed applicant for KOKO SPIROMETER?

The FDA 510(k) record lists Ferraris Respiratory, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOKO SPIROMETER?

The FDA product code for KOKO 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 Ferraris Respiratory, Inc. 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.

K022276KOKOMATE

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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