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FDA 510(k)

FERRIS POLYMEM SILVER WOUND DRESSING

K-Number: K031307 · 2003-10-22

ApplicantFerris Mfg. Corp.
Decision Date2003-10-22
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

FERRIS POLYMEM SILVER WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 2003-10-22 under 510(k) number K031307. 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 FERRIS POLYMEM SILVER WOUND DRESSING?

FERRIS POLYMEM SILVER WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2003-10-22. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K031307.

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

FERRIS POLYMEM SILVER WOUND DRESSING received FDA 510(k) clearance on 2003-10-22, under 510(k) number K031307.

Who is the listed applicant for FERRIS POLYMEM SILVER WOUND DRESSING?

The FDA 510(k) record lists Ferris Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FERRIS POLYMEM SILVER WOUND DRESSING?

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

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Other records listing Ferris Mfg. Corp. 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.

K031660FERRIS POLYMEM STERILE BREAST PADK002129FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGENK991729FERRIS POLYOSTOMY STERILE WOUND DRESSINGK990906FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLERK984539FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSINGK982306POLYTUBE

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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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