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FDA 510(k)

MERITS MODEL N SERIES NEBULIZER COMPRESSORS

K-Number: K092859 · 2010-07-02

Decision Date2010-07-02
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERITS MODEL N SERIES NEBULIZER COMPRESSORS is the device name listed in this FDA 510(k) record. The listed applicant is Merits Health Products Co., Ltd.. It received FDA 510(k) clearance on 2010-07-02 under 510(k) number K092859. 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 MERITS MODEL N SERIES NEBULIZER COMPRESSORS?

MERITS MODEL N SERIES NEBULIZER COMPRESSORS is a medical device that received FDA 510(k) clearance on 2010-07-02. The listed applicant is Merits Health Products Co., Ltd.. The 510(k) number is K092859.

When did MERITS MODEL N SERIES NEBULIZER COMPRESSORS receive FDA 510(k) clearance?

MERITS MODEL N SERIES NEBULIZER COMPRESSORS received FDA 510(k) clearance on 2010-07-02, under 510(k) number K092859.

Who is the listed applicant for MERITS MODEL N SERIES NEBULIZER COMPRESSORS?

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

What is the FDA product code for MERITS MODEL N SERIES NEBULIZER COMPRESSORS?

The FDA product code for MERITS MODEL N SERIES NEBULIZER COMPRESSORS 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 Merits Health Products 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.

View all 17 devices →

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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