UNIWEB, VERSION 5.0
K-Number: K071166 · 2007-07-23
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Device Summary
Frequently Asked Questions
What is the UNIWEB, VERSION 5.0?
UNIWEB, VERSION 5.0 is a medical device that received FDA 510(k) clearance on 2007-07-23. The listed applicant is Electronic Business Machine Co., Ltd. (Ebm). The 510(k) number is K071166.
When did UNIWEB, VERSION 5.0 receive FDA 510(k) clearance?
UNIWEB, VERSION 5.0 received FDA 510(k) clearance on 2007-07-23, under 510(k) number K071166.
Who is the listed applicant for UNIWEB, VERSION 5.0?
The FDA 510(k) record lists Electronic Business Machine Co., Ltd. (Ebm) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIWEB, VERSION 5.0?
The FDA product code for UNIWEB, VERSION 5.0 is LLZ.
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 Electronic Business Machine Co., Ltd. (Ebm) 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: LLZ)
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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