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FDA 510(k)

HUMIDIFIER FILTER

K-Number: K780535 · 1978-04-27

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1978-04-27
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HUMIDIFIER FILTER 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 1978-04-27 under 510(k) number K780535. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMIDIFIER FILTER?

HUMIDIFIER FILTER is a medical device that received FDA 510(k) clearance on 1978-04-27. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K780535.

When did HUMIDIFIER FILTER receive FDA 510(k) clearance?

HUMIDIFIER FILTER received FDA 510(k) clearance on 1978-04-27, under 510(k) number K780535.

Who is the listed applicant for HUMIDIFIER FILTER?

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 HUMIDIFIER FILTER?

The FDA product code for HUMIDIFIER FILTER is CAH.

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Other records listing Hudson Oxygen Therapy Sales Co. as applicant

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Related Devices (Code: CAH)

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.

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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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