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FDA 510(k)

Ross Ru Wound Dressing Gel

K-Number: K162017 · 2017-04-20

ApplicantBiotd S.A.
Decision Date2017-04-20
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

Ross Ru Wound Dressing Gel is the device name listed in this FDA 510(k) record. The listed applicant is Biotd S.A.. It received FDA 510(k) clearance on 2017-04-20 under 510(k) number K162017. 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 Ross Ru Wound Dressing Gel?

Ross Ru Wound Dressing Gel is a medical device that received FDA 510(k) clearance on 2017-04-20. The listed applicant is Biotd S.A.. The 510(k) number is K162017.

When did Ross Ru Wound Dressing Gel receive FDA 510(k) clearance?

Ross Ru Wound Dressing Gel received FDA 510(k) clearance on 2017-04-20, under 510(k) number K162017.

Who is the listed applicant for Ross Ru Wound Dressing Gel?

The FDA 510(k) record lists Biotd S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ross Ru Wound Dressing Gel?

The FDA product code for Ross Ru Wound Dressing Gel 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

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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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