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FDA 510(k)

ReminGel

K-Number: K241489 · 2025-01-08

ApplicantInter-Med, Inc.
Decision Date2025-01-08
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the ReminGel?

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

When was ReminGel approved by the FDA?

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

What company makes ReminGel?

ReminGel is manufactured by Inter-Med, Inc..

What is the FDA product code for ReminGel?

The FDA product code for ReminGel is LBH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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