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FDA 510(k)

VITALOGRAPH-EC60 HYDROGEN MONITOR

K-Number: K874892 · 1988-06-02

ApplicantVitalograph , Ltd.
Decision Date1988-06-02
Product CodeNRH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VITALOGRAPH-EC60 HYDROGEN MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Vitalograph , Ltd.. It received FDA 510(k) clearance on 1988-06-02 under 510(k) number K874892. The device is classified under product code NRH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALOGRAPH-EC60 HYDROGEN MONITOR?

VITALOGRAPH-EC60 HYDROGEN MONITOR is a medical device that received FDA 510(k) clearance on 1988-06-02. The listed applicant is Vitalograph , Ltd.. The 510(k) number is K874892.

When did VITALOGRAPH-EC60 HYDROGEN MONITOR receive FDA 510(k) clearance?

VITALOGRAPH-EC60 HYDROGEN MONITOR received FDA 510(k) clearance on 1988-06-02, under 510(k) number K874892.

Who is the listed applicant for VITALOGRAPH-EC60 HYDROGEN MONITOR?

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 VITALOGRAPH-EC60 HYDROGEN MONITOR?

The FDA product code for VITALOGRAPH-EC60 HYDROGEN MONITOR is NRH.

Related Clinical Trials

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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 INTERFACEK925085ESCORT SPIROMETERK930085VITALOGRAPH DATA STORAGE SPIROMETERK912412VITALOGRAPH SPIROTRAC IIIK893665AEROSOL INHALATION MONITOR

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Related Devices (Code: NRH)

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.

K033688MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITYMicro Direct, Inc.K963376MICRO H2Micro Direct, Inc.K882499JAYCO HYDROGEN MONITOREnteron, Inc.

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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