EMG AC/DC SUCTION UNIT
K-Number: K063448 · 2006-11-30
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Device Summary
Frequently Asked Questions
What is the EMG AC/DC SUCTION UNIT?
EMG AC/DC SUCTION UNIT is a medical device that received FDA 510(k) clearance on 2006-11-30. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K063448.
When did EMG AC/DC SUCTION UNIT receive FDA 510(k) clearance?
EMG AC/DC SUCTION UNIT received FDA 510(k) clearance on 2006-11-30, under 510(k) number K063448.
Who is the listed applicant for EMG AC/DC SUCTION UNIT?
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 AC/DC SUCTION UNIT?
The FDA product code for EMG AC/DC SUCTION UNIT is JCX.
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: JCX)
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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