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FDA 510(k)

IN-THE NEBULIZER

K-Number: K900470 · 1990-05-18

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1990-05-18
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IN-THE NEBULIZER 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 1990-05-18 under 510(k) number K900470. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN-THE NEBULIZER?

IN-THE NEBULIZER is a medical device that received FDA 510(k) clearance on 1990-05-18. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K900470.

When did IN-THE NEBULIZER receive FDA 510(k) clearance?

IN-THE NEBULIZER received FDA 510(k) clearance on 1990-05-18, under 510(k) number K900470.

Who is the listed applicant for IN-THE NEBULIZER?

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 IN-THE NEBULIZER?

The FDA product code for IN-THE NEBULIZER is CAF.

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Other records listing Hudson Oxygen Therapy Sales Co. as applicant

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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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