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FDA 510(k)

DEVILBISS NEBULIZER MODEL 800

K-Number: K993492 · 2000-04-21

ApplicantSunrise Medical Hhg, Inc.
Decision Date2000-04-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DEVILBISS NEBULIZER MODEL 800 is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical Hhg, Inc.. It received FDA 510(k) clearance on 2000-04-21 under 510(k) number K993492. 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 DEVILBISS NEBULIZER MODEL 800?

DEVILBISS NEBULIZER MODEL 800 is a medical device that received FDA 510(k) clearance on 2000-04-21. The listed applicant is Sunrise Medical Hhg, Inc.. The 510(k) number is K993492.

When did DEVILBISS NEBULIZER MODEL 800 receive FDA 510(k) clearance?

DEVILBISS NEBULIZER MODEL 800 received FDA 510(k) clearance on 2000-04-21, under 510(k) number K993492.

Who is the listed applicant for DEVILBISS NEBULIZER MODEL 800?

The FDA 510(k) record lists Sunrise Medical Hhg, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEVILBISS NEBULIZER MODEL 800?

The FDA product code for DEVILBISS NEBULIZER MODEL 800 is CAF.

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Related Devices (Code: 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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