FDA 510(k)

Pulse Aloe-ahh

K号: K152671 · 2016-07-11

决定日期2016-07-11

产品代码NUC

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决定实质等同

器械摘要

Pulse Aloe-ahh is the device name listed in this FDA 510(k) record. The listed applicant is Toaster Labs, Inc.. It received FDA 510(k) clearance on 2016-07-11 under 510(k) number K152671. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Pulse Aloe-ahh?

Pulse Aloe-ahh is a medical device that received FDA 510(k) clearance on 2016-07-11. The listed applicant is Toaster Labs, Inc.. The 510(k) number is K152671.

When did Pulse Aloe-ahh receive FDA 510(k) clearance?

Pulse Aloe-ahh received FDA 510(k) clearance on 2016-07-11, under 510(k) number K152671.

Who is the listed applicant for Pulse Aloe-ahh?

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

What is the FDA product code for Pulse Aloe-ahh?

The FDA product code for Pulse Aloe-ahh is NUC.

列明Toaster Labs, 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。

K152628Pulse H20h!

官方来源

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