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FDA 510(k)

FERRIS POLYMEM HYDROPHILIC WOUND DRESSING

K-Number: K932913 · 1994-06-07

ApplicantFerris Mfg. Corp.
Decision Date1994-06-07
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

FERRIS POLYMEM HYDROPHILIC 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 1994-06-07 under 510(k) number K932913. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the FERRIS POLYMEM HYDROPHILIC WOUND DRESSING?

FERRIS POLYMEM HYDROPHILIC WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-06-07. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K932913.

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

FERRIS POLYMEM HYDROPHILIC WOUND DRESSING received FDA 510(k) clearance on 1994-06-07, under 510(k) number K932913.

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

The FDA product code for FERRIS POLYMEM HYDROPHILIC WOUND DRESSING is KMF.

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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 PADK031307FERRIS POLYMEM SILVER WOUND DRESSINGK002129FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGENK991729FERRIS POLYOSTOMY STERILE WOUND DRESSINGK990906FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLERK984539FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING

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Related Devices (Code: KMF)

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, 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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