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FDA 510(k)

RECORDER, CHART, MODEL 5536

K-Number: K770342 · 1977-03-01

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1977-03-01
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECORDER, CHART, MODEL 5536 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 1977-03-01 under 510(k) number K770342. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECORDER, CHART, MODEL 5536?

RECORDER, CHART, MODEL 5536 is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K770342.

When did RECORDER, CHART, MODEL 5536 receive FDA 510(k) clearance?

RECORDER, CHART, MODEL 5536 received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770342.

Who is the listed applicant for RECORDER, CHART, MODEL 5536?

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 RECORDER, CHART, MODEL 5536?

The FDA product code for RECORDER, CHART, MODEL 5536 is DSF.

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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: DSF)

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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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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