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FDA 510(k)

WOUND DRESSING

K-Number: K896702 · 1990-01-19

ApplicantViaderm Pharmaceuticals, Inc.
Decision Date1990-01-19
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Viaderm Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1990-01-19 under 510(k) number K896702. 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 WOUND DRESSING?

WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Viaderm Pharmaceuticals, Inc.. The 510(k) number is K896702.

When did WOUND DRESSING receive FDA 510(k) clearance?

WOUND DRESSING received FDA 510(k) clearance on 1990-01-19, under 510(k) number K896702.

Who is the listed applicant for WOUND DRESSING?

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

What is the FDA product code for WOUND DRESSING?

The FDA product code for WOUND DRESSING is FRO. This falls under the Anesthesiology category.

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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.

K254168Actolind® (06.3637. Actolind® Gel Plus)ACTO GmbHK254041SkinSmart Antimicrobial HydroGelMagic Science Supply, LLCK261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, 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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