Avara Viewer
K号: K262120 · 2026-07-10
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器械摘要
Avara Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Avara Software. It received FDA 510(k) clearance on 2026-07-10 under 510(k) number K262120. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Avara Viewer?
Avara Viewer is a medical device that received FDA 510(k) clearance on 2026-07-10. The listed applicant is Avara Software. The 510(k) number is K262120.
When did Avara Viewer receive FDA 510(k) clearance?
Avara Viewer received FDA 510(k) clearance on 2026-07-10, under 510(k) number K262120.
Who is the listed applicant for Avara Viewer?
The FDA 510(k) record lists Avara Software as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Avara Viewer?
The FDA product code for Avara Viewer is LLZ.
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相关器械（代码：LLZ）
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官方来源
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