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FDA 510(k)

AEROSOL EFFUSION SYSTEM #1740

K-Number: K770771 · 1977-06-02

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1977-06-02
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AEROSOL EFFUSION SYSTEM #1740 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 1977-06-02 under 510(k) number K770771. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROSOL EFFUSION SYSTEM #1740?

AEROSOL EFFUSION SYSTEM #1740 is a medical device that received FDA 510(k) clearance on 1977-06-02. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K770771.

When did AEROSOL EFFUSION SYSTEM #1740 receive FDA 510(k) clearance?

AEROSOL EFFUSION SYSTEM #1740 received FDA 510(k) clearance on 1977-06-02, under 510(k) number K770771.

Who is the listed applicant for AEROSOL EFFUSION SYSTEM #1740?

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 AEROSOL EFFUSION SYSTEM #1740?

The FDA product code for AEROSOL EFFUSION SYSTEM #1740 is BYH.

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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. MONITORK895231CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER

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Related Devices (Code: BYH)

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.

K946057AQUALARM MOISTURE SENSOR MODEL P85000Pegasus Research Corp.K932722CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEMCarie Med-Tech Services, Inc.K921624DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITSIntertech Resources, Inc.K900047THAYER SUCTION EVACUATION CONDENSATE COLLECTIONThayer Medical Corp.K897057THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEMThayer Medical Corp.K900591VENT-TRAP CAT# WR1000Ventlab Corp.

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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