FDA 510(k)

Ampa One系统（AMPA-001）

K号: K243319 · 2025-02-13

申请人Neuromodulatory Devices & Applications

决定日期2025-02-13

产品代码OBP

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决定实质等同

器械摘要

Ampa One System (AMPA-001) is the device name listed in this FDA 510(k) record. The listed applicant is Neuromodulatory Devices & Applications. It received FDA 510(k) clearance on 2025-02-13 under 510(k) number K243319. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Ampa One System (AMPA-001)?

Ampa One System (AMPA-001) is a medical device that received FDA 510(k) clearance on 2025-02-13. The listed applicant is Neuromodulatory Devices & Applications. The 510(k) number is K243319.

When did Ampa One System (AMPA-001) receive FDA 510(k) clearance?

Ampa One System (AMPA-001) received FDA 510(k) clearance on 2025-02-13, under 510(k) number K243319.

Who is the listed applicant for Ampa One System (AMPA-001)?

The FDA 510(k) record lists Neuromodulatory Devices & Applications as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ampa One System (AMPA-001)?

The FDA product code for Ampa One System (AMPA-001) is OBP.

列明Neuromodulatory Devices & Applications为申报人的其他记录

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K251210Ampa One系统（AMPA-001）

官方来源

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