FDA 510(k)

JetBoots PRO Plus

K号: K241256 · 2024-08-30

决定日期2024-08-30

产品代码IRP

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决定实质等同

器械摘要

JetBoots PRO Plus is the device name listed in this FDA 510(k) record. The listed applicant is Therabody, Inc.. It received FDA 510(k) clearance on 2024-08-30 under 510(k) number K241256. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the JetBoots PRO Plus?

JetBoots PRO Plus is a medical device that received FDA 510(k) clearance on 2024-08-30. The listed applicant is Therabody, Inc.. The 510(k) number is K241256.

When did JetBoots PRO Plus receive FDA 510(k) clearance?

JetBoots PRO Plus received FDA 510(k) clearance on 2024-08-30, under 510(k) number K241256.

Who is the listed applicant for JetBoots PRO Plus?

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

What is the FDA product code for JetBoots PRO Plus?

The FDA product code for JetBoots PRO Plus is IRP.

列明Therabody, 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。

K230293TheraFace口罩

相关器械（代码：IRP）

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。

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