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FDA 510(k)

LIFELINE 4800-C DIGITAL SPIROMETER

K-Number: K822861 · 1982-11-03

ApplicantLifeline Controls
Decision Date1982-11-03
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFELINE 4800-C DIGITAL SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lifeline Controls. It received FDA 510(k) clearance on 1982-11-03 under 510(k) number K822861. 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 LIFELINE 4800-C DIGITAL SPIROMETER?

LIFELINE 4800-C DIGITAL SPIROMETER is a medical device that received FDA 510(k) clearance on 1982-11-03. The listed applicant is Lifeline Controls. The 510(k) number is K822861.

When did LIFELINE 4800-C DIGITAL SPIROMETER receive FDA 510(k) clearance?

LIFELINE 4800-C DIGITAL SPIROMETER received FDA 510(k) clearance on 1982-11-03, under 510(k) number K822861.

Who is the listed applicant for LIFELINE 4800-C DIGITAL SPIROMETER?

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

What is the FDA product code for LIFELINE 4800-C DIGITAL SPIROMETER?

The FDA product code for LIFELINE 4800-C DIGITAL 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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