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FDA 510(k)

DISPOSABLE MEDICATION NEBULIZER

K-Number: K801867 · 1980-08-20

ApplicantHospitax
Decision Date1980-08-20
Product CodeLCQ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE MEDICATION NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Hospitax. It received FDA 510(k) clearance on 1980-08-20 under 510(k) number K801867. The device is classified under product code LCQ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE MEDICATION NEBULIZER?

DISPOSABLE MEDICATION NEBULIZER is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Hospitax. The 510(k) number is K801867.

When did DISPOSABLE MEDICATION NEBULIZER receive FDA 510(k) clearance?

DISPOSABLE MEDICATION NEBULIZER received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801867.

Who is the listed applicant for DISPOSABLE MEDICATION NEBULIZER?

The FDA 510(k) record lists Hospitax as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE MEDICATION NEBULIZER?

The FDA product code for DISPOSABLE MEDICATION NEBULIZER is LCQ.

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Related Devices (Code: LCQ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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