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FDA 510(k)

DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM

K-Number: K020900 · 2002-06-03

ApplicantSunrise Medical Hhg, Inc.
Decision Date2002-06-03
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM 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 2002-06-03 under 510(k) number K020900. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM?

DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM is a medical device that received FDA 510(k) clearance on 2002-06-03. The listed applicant is Sunrise Medical Hhg, Inc.. The 510(k) number is K020900.

When did DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM receive FDA 510(k) clearance?

DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM received FDA 510(k) clearance on 2002-06-03, under 510(k) number K020900.

Who is the listed applicant for DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM?

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 MODEL 9200D HEATED HUMIDIFIER SYSTEM?

The FDA product code for DEVILBISS MODEL 9200D HEATED HUMIDIFIER SYSTEM is BTT.

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Other records listing Sunrise Medical Hhg, Inc. as applicant

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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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