UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0
K-Number: K062743 · 2006-10-31
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Device Summary
Frequently Asked Questions
What is the UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0?
UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0 is a medical device that received FDA 510(k) clearance on 2006-10-31. The listed applicant is Electronic Business Machine Co., Ltd. (Ebm). The 510(k) number is K062743.
When did UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0 receive FDA 510(k) clearance?
UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0 received FDA 510(k) clearance on 2006-10-31, under 510(k) number K062743.
Who is the listed applicant for UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0?
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 UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0?
The FDA product code for UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0 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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