ART.1-US
K号: K253078 · 2026-05-14
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器械摘要
ART.1-US is the device name listed in this FDA 510(k) record. The listed applicant is Seetreat Pty, Ltd.. It received FDA 510(k) clearance on 2026-05-14 under 510(k) number K253078. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ART.1-US?
ART.1-US is a medical device that received FDA 510(k) clearance on 2026-05-14. The listed applicant is Seetreat Pty, Ltd.. The 510(k) number is K253078.
When did ART.1-US receive FDA 510(k) clearance?
ART.1-US received FDA 510(k) clearance on 2026-05-14, under 510(k) number K253078.
Who is the listed applicant for ART.1-US?
The FDA 510(k) record lists Seetreat Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ART.1-US?
The FDA product code for ART.1-US is MUJ.
相关器械（代码：MUJ）
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官方来源
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