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FDA 510(k)

EMG HANDLE NEBULIZER NB02 SERIES

K-Number: K052438 · 2006-01-31

Decision Date2006-01-31
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMG HANDLE NEBULIZER NB02 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 2006-01-31 under 510(k) number K052438. 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 EMG HANDLE NEBULIZER NB02 SERIES?

EMG HANDLE NEBULIZER NB02 SERIES is a medical device that received FDA 510(k) clearance on 2006-01-31. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K052438.

When did EMG HANDLE NEBULIZER NB02 SERIES receive FDA 510(k) clearance?

EMG HANDLE NEBULIZER NB02 SERIES received FDA 510(k) clearance on 2006-01-31, under 510(k) number K052438.

Who is the listed applicant for EMG HANDLE NEBULIZER NB02 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 EMG HANDLE NEBULIZER NB02 SERIES?

The FDA product code for EMG HANDLE NEBULIZER NB02 SERIES 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 Emg Technology 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 11 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

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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