EMG HANDLE NEBULIZER NB02 SERIES
K-Number: K052438 · 2006-01-31
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Device Summary
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.
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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