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FDA 510(k)

PERFILM MEMBRANE DRESSING

K-Number: K822467 · 1982-12-30

ApplicantChesebrough-Pond'S U.S.A. Co.
Decision Date1982-12-30
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

PERFILM MEMBRANE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K822467. 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 PERFILM MEMBRANE DRESSING?

PERFILM MEMBRANE DRESSING is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K822467.

When did PERFILM MEMBRANE DRESSING receive FDA 510(k) clearance?

PERFILM MEMBRANE DRESSING received FDA 510(k) clearance on 1982-12-30, under 510(k) number K822467.

Who is the listed applicant for PERFILM MEMBRANE DRESSING?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERFILM MEMBRANE DRESSING?

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

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Other records listing Chesebrough-Pond'S U.S.A. Co. 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.

K863866RESPIRADYNE II(TM)K862803CHESEBROUGH POND'S HYDROCOLLOID DRESSINGK851383BLISTERFILM TRANSPARENT DRESSINGK851382CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSINGK851539CHESEBROUGH-PONDS KANGAROO PUMP SET W/EASY-CAP CLOK843567KANGAROO NASOGASTRIC FEEDING TUBE

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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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