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FDA 510(k)

FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER

K-Number: K990906 · 1999-04-29

ApplicantFerris Mfg. Corp.
Decision Date1999-04-29
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER 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 1999-04-29 under 510(k) number K990906. 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 POLYWIC STERILE CAVITY WOUND FILLER?

FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER is a medical device that received FDA 510(k) clearance on 1999-04-29. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K990906.

When did FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER receive FDA 510(k) clearance?

FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER received FDA 510(k) clearance on 1999-04-29, under 510(k) number K990906.

Who is the listed applicant for FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER?

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 POLYWIC STERILE CAVITY WOUND FILLER?

The FDA product code for FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER 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 DRESSINGK984539FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSINGK982306POLYTUBE

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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.

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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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