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FDA 510(k)

ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING

K-Number: K022483 · 2003-02-03

ApplicantJohnson & Johnson Medical, Ltd.
Decision Date2003-02-03
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Ltd.. It received FDA 510(k) clearance on 2003-02-03 under 510(k) number K022483. 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 ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING?

ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING is a medical device that received FDA 510(k) clearance on 2003-02-03. The listed applicant is Johnson & Johnson Medical, Ltd.. The 510(k) number is K022483.

When did ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING receive FDA 510(k) clearance?

ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING received FDA 510(k) clearance on 2003-02-03, under 510(k) number K022483.

Who is the listed applicant for ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING?

The FDA 510(k) record lists Johnson & Johnson Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING?

The FDA product code for ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING is FRO. This falls under the Anesthesiology category.

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Other records listing Johnson & Johnson Medical, Ltd. as applicant

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.

K033523COLLAGEN-ORC ANTIMICROBIAL MATRIXK014129PROMOGRAN MATRIX WOUND DRESSING

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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