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FDA 510(k)

SIDESTREAM NEBULIZER

K-Number: K991725 · 1999-07-30

ApplicantInspired Medical Products , Ltd.
Decision Date1999-07-30
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIDESTREAM NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Inspired Medical Products , Ltd.. It received FDA 510(k) clearance on 1999-07-30 under 510(k) number K991725. 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 SIDESTREAM NEBULIZER?

SIDESTREAM NEBULIZER is a medical device that received FDA 510(k) clearance on 1999-07-30. The listed applicant is Inspired Medical Products , Ltd.. The 510(k) number is K991725.

When did SIDESTREAM NEBULIZER receive FDA 510(k) clearance?

SIDESTREAM NEBULIZER received FDA 510(k) clearance on 1999-07-30, under 510(k) number K991725.

Who is the listed applicant for SIDESTREAM NEBULIZER?

The FDA 510(k) record lists Inspired Medical Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIDESTREAM NEBULIZER?

The FDA product code for SIDESTREAM NEBULIZER is CAF.

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Official Source

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