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FDA 510(k)

FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)

K-Number: K900127 · 1990-05-18

ApplicantFerris Mfg. Corp.
Decision Date1990-05-18
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS) 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 1990-05-18 under 510(k) number K900127. 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 HYDROPHILIC DRESSING (ADD'L INDICATIONS)?

FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS) is a medical device that received FDA 510(k) clearance on 1990-05-18. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K900127.

When did FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS) receive FDA 510(k) clearance?

FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS) received FDA 510(k) clearance on 1990-05-18, under 510(k) number K900127.

Who is the listed applicant for FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)?

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 HYDROPHILIC DRESSING (ADD'L INDICATIONS)?

The FDA product code for FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS) 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.

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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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