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FDA 510(k)

DEVILBISS AP-50 COMPRESSOR/NEBULIZER

K-Number: K900602 · 1990-04-23

ApplicantDevilbiss Health Care, Inc.
Decision Date1990-04-23
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DEVILBISS AP-50 COMPRESSOR/NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Devilbiss Health Care, Inc.. It received FDA 510(k) clearance on 1990-04-23 under 510(k) number K900602. 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 AP-50 COMPRESSOR/NEBULIZER?

DEVILBISS AP-50 COMPRESSOR/NEBULIZER is a medical device that received FDA 510(k) clearance on 1990-04-23. The listed applicant is Devilbiss Health Care, Inc.. The 510(k) number is K900602.

When did DEVILBISS AP-50 COMPRESSOR/NEBULIZER receive FDA 510(k) clearance?

DEVILBISS AP-50 COMPRESSOR/NEBULIZER received FDA 510(k) clearance on 1990-04-23, under 510(k) number K900602.

Who is the listed applicant for DEVILBISS AP-50 COMPRESSOR/NEBULIZER?

The FDA 510(k) record lists Devilbiss Health Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEVILBISS AP-50 COMPRESSOR/NEBULIZER?

The FDA product code for DEVILBISS AP-50 COMPRESSOR/NEBULIZER is BTT.

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Other records listing Devilbiss Health Care, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K963349DEVILBISS 8650DK970289COMPRESSOR/NEBULIZER #3650K961126PULSE DOSE SERIESK950849MODEL #7354K952491MODEL 7355K952249JET NEBULIZER

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Related Devices (Code: BTT)

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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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