FDA 510(k)

NeurotriS (SX2500); NeurotriS (SX3800)

K号: K251909 · 2025-09-03

决定日期2025-09-03

产品代码NFO

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决定实质等同

器械摘要

NeurotriS (SX2500); NeurotriS (SX3800) is the device name listed in this FDA 510(k) record. The listed applicant is A-1 Engineering. It received FDA 510(k) clearance on 2025-09-03 under 510(k) number K251909. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the NeurotriS (SX2500); NeurotriS (SX3800)?

NeurotriS (SX2500); NeurotriS (SX3800) is a medical device that received FDA 510(k) clearance on 2025-09-03. The listed applicant is A-1 Engineering. The 510(k) number is K251909.

When did NeurotriS (SX2500); NeurotriS (SX3800) receive FDA 510(k) clearance?

NeurotriS (SX2500); NeurotriS (SX3800) received FDA 510(k) clearance on 2025-09-03, under 510(k) number K251909.

Who is the listed applicant for NeurotriS (SX2500); NeurotriS (SX3800)?

The FDA 510(k) record lists A-1 Engineering as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NeurotriS (SX2500); NeurotriS (SX3800)?

The FDA product code for NeurotriS (SX2500); NeurotriS (SX3800) is NFO.

列明A-1 Engineering为申报人的其他记录

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