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FDA 510(k)

MONITOR 5590- ANALYZER 5595EC

K-Number: K840565 · 1984-04-02

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1984-04-02
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONITOR 5590- ANALYZER 5595EC is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Oxygen Therapy Sales Co.. It received FDA 510(k) clearance on 1984-04-02 under 510(k) number K840565. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITOR 5590- ANALYZER 5595EC?

MONITOR 5590- ANALYZER 5595EC is a medical device that received FDA 510(k) clearance on 1984-04-02. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K840565.

When did MONITOR 5590- ANALYZER 5595EC receive FDA 510(k) clearance?

MONITOR 5590- ANALYZER 5595EC received FDA 510(k) clearance on 1984-04-02, under 510(k) number K840565.

Who is the listed applicant for MONITOR 5590- ANALYZER 5595EC?

The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONITOR 5590- ANALYZER 5595EC?

The FDA product code for MONITOR 5590- ANALYZER 5595EC is CCL.

Related Clinical Trials

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Other records listing Hudson Oxygen Therapy Sales Co. 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.

K902062PEEP VALVEK900783MDI ADAPTORK900470IN-THE NEBULIZERK895589MANUAL RESUSCITATORK896136INFANT C.P.A.P. MONITORK895747VENTILARM II PORTABLE AIRWAY PRESSURE MONITOR

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Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, 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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