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FDA 510(k)

QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER

K-Number: K112824 · 2012-06-21

ApplicantQuality Life Technologies Co;Ltd
Decision Date2012-06-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Quality Life Technologies Co;Ltd. It received FDA 510(k) clearance on 2012-06-21 under 510(k) number K112824. 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 QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER?

QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER is a medical device that received FDA 510(k) clearance on 2012-06-21. The listed applicant is Quality Life Technologies Co;Ltd. The 510(k) number is K112824.

When did QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER receive FDA 510(k) clearance?

QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER received FDA 510(k) clearance on 2012-06-21, under 510(k) number K112824.

Who is the listed applicant for QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER?

The FDA 510(k) record lists Quality Life Technologies Co;Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER?

The FDA product code for QUALITY LIFE TECHNOLOGIES COMPRESSOR NEBULIZER is CAF.

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Related Devices (Code: CAF)

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.

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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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