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FDA 510(k)

Derma-R Cream (Derma-R Cream)

K-Number: K240722 · 2024-09-20

ApplicantRaya Pharmaceuticals, LLC
Decision Date2024-09-20
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

Derma-R Cream (Derma-R Cream) is the device name listed in this FDA 510(k) record. The listed applicant is Raya Pharmaceuticals, LLC. It received FDA 510(k) clearance on 2024-09-20 under 510(k) number K240722. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Derma-R Cream (Derma-R Cream)?

Derma-R Cream (Derma-R Cream) is a medical device that received FDA 510(k) clearance on 2024-09-20. The listed applicant is Raya Pharmaceuticals, LLC. The 510(k) number is K240722.

When did Derma-R Cream (Derma-R Cream) receive FDA 510(k) clearance?

Derma-R Cream (Derma-R Cream) received FDA 510(k) clearance on 2024-09-20, under 510(k) number K240722.

Who is the listed applicant for Derma-R Cream (Derma-R Cream)?

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

What is the FDA product code for Derma-R Cream (Derma-R Cream)?

The FDA product code for Derma-R Cream (Derma-R Cream) is FRO. This falls under the Anesthesiology category.

Related Devices (Code: FRO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, Inc.K251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261638Bonvadis®Oneness Biotech Co., Ltd.K254073StatSeal DiscMerit Medical Systems, Inc.

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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