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FDA 510(k)

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

K-Number: K895231 · 1989-10-27

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1989-10-27
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CATALOG NO. 1755 1S0-NEB, A FILTERED 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 1989-10-27 under 510(k) number K895231. 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 CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER?

CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER is a medical device that received FDA 510(k) clearance on 1989-10-27. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K895231.

When did CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER receive FDA 510(k) clearance?

CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER received FDA 510(k) clearance on 1989-10-27, under 510(k) number K895231.

Who is the listed applicant for CATALOG NO. 1755 1S0-NEB, A FILTERED 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 CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER?

The FDA product code for CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER is CAF.

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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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