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FDA 510(k)

COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES

K-Number: K043238 · 2005-07-06

ApplicantEmg Technology Co., Ltd.
Decision Date2005-07-06
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Emg Technology Co., Ltd.. It received FDA 510(k) clearance on 2005-07-06 under 510(k) number K043238. 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 COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES?

COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES is a medical device that received FDA 510(k) clearance on 2005-07-06. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K043238.

When did COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES receive FDA 510(k) clearance?

COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES received FDA 510(k) clearance on 2005-07-06, under 510(k) number K043238.

Who is the listed applicant for COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES?

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

What is the FDA product code for COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES?

The FDA product code for COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES 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

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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