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FDA 510(k)

ESCORT SPIROMETER

K-Number: K925085 · 1993-08-12

ApplicantVitalograph , Ltd.
Decision Date1993-08-12
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ESCORT SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Vitalograph , Ltd.. It received FDA 510(k) clearance on 1993-08-12 under 510(k) number K925085. 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 ESCORT SPIROMETER?

ESCORT SPIROMETER is a medical device that received FDA 510(k) clearance on 1993-08-12. The listed applicant is Vitalograph , Ltd.. The 510(k) number is K925085.

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

ESCORT SPIROMETER received FDA 510(k) clearance on 1993-08-12, under 510(k) number K925085.

Who is the listed applicant for ESCORT SPIROMETER?

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

What is the FDA product code for ESCORT SPIROMETER?

The FDA product code for ESCORT SPIROMETER is BZG.

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Other records listing Vitalograph , Ltd. 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.

K253293VitaloJAK Clinic (Model 7100)K950854VITALOGRAPH 2110 SOFTWARE INTERFACEK930085VITALOGRAPH DATA STORAGE SPIROMETERK912412VITALOGRAPH SPIROTRAC IIIK893665AEROSOL INHALATION MONITORK892524VITALOGRAPH-BREATHCO MONITOR

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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

View on FDA Database →

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

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