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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 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.

Frequently Asked Questions

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.

Other records listing Inter-Med, Inc. as applicant

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Official Source

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

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