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FDA 510(k)

C300 SERIES AIR NEBULIZER COMPRESSOR

K-Number: K062952 · 2007-02-21

Decision Date2007-02-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

C300 SERIES AIR NEBULIZER COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Choice Smart Health Care Co. , Ltd.. It received FDA 510(k) clearance on 2007-02-21 under 510(k) number K062952. 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 C300 SERIES AIR NEBULIZER COMPRESSOR?

C300 SERIES AIR NEBULIZER COMPRESSOR is a medical device that received FDA 510(k) clearance on 2007-02-21. The listed applicant is Choice Smart Health Care Co. , Ltd.. The 510(k) number is K062952.

When did C300 SERIES AIR NEBULIZER COMPRESSOR receive FDA 510(k) clearance?

C300 SERIES AIR NEBULIZER COMPRESSOR received FDA 510(k) clearance on 2007-02-21, under 510(k) number K062952.

Who is the listed applicant for C300 SERIES AIR NEBULIZER COMPRESSOR?

The FDA 510(k) record lists Choice Smart Health Care Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C300 SERIES AIR NEBULIZER COMPRESSOR?

The FDA product code for C300 SERIES AIR NEBULIZER COMPRESSOR is CAF.

Related Clinical Trials

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.

Other records listing Choice Smart Health Care Co. , Ltd. 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.

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.

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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