FDA 510(k)

ReminGel

K号: K241489 · 2025-01-08

决定日期2025-01-08

产品代码LBH

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决定实质等同

器械摘要

ReminGel is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med, Inc.. It received FDA 510(k) clearance on 2025-01-08 under 510(k) number K241489. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ReminGel?

ReminGel is a medical device that received FDA 510(k) clearance on 2025-01-08. The listed applicant is Inter-Med, Inc.. The 510(k) number is K241489.

When did ReminGel receive FDA 510(k) clearance?

ReminGel received FDA 510(k) clearance on 2025-01-08, under 510(k) number K241489.

Who is the listed applicant for ReminGel?

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

What is the FDA product code for ReminGel?

The FDA product code for ReminGel is LBH.

列明Inter-Med, 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。

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