FDA 510(k)

ANSiStim-PP

K号: K220397 · 2022-05-12

决定日期2022-05-12

产品代码NHI

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决定实质等同

器械摘要

ANSiStim-PP is the device name listed in this FDA 510(k) record. The listed applicant is Dyansys, Inc.. It received FDA 510(k) clearance on 2022-05-12 under 510(k) number K220397. The device is classified under product code NHI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ANSiStim-PP?

ANSiStim-PP is a medical device that received FDA 510(k) clearance on 2022-05-12. The listed applicant is Dyansys, Inc.. The 510(k) number is K220397.

When did ANSiStim-PP receive FDA 510(k) clearance?

ANSiStim-PP received FDA 510(k) clearance on 2022-05-12, under 510(k) number K220397.

Who is the listed applicant for ANSiStim-PP?

The FDA 510(k) record lists Dyansys, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANSiStim-PP?

The FDA product code for ANSiStim-PP is NHI.

列明Dyansys, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K221425主要缓解 K221231Drug Relief v1 K213188主要缓解 K212859First Relief K211971Drug Relief v1 K202940First Relief v1

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