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FDA 510(k)

CAVI-CARE CONFORMING FOAM DRESSING

K-Number: K943619 · 1994-08-19

ApplicantSmith & Nephew United, Inc.
Decision Date1994-08-19
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

CAVI-CARE CONFORMING FOAM DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew United, Inc.. It received FDA 510(k) clearance on 1994-08-19 under 510(k) number K943619. 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 CAVI-CARE CONFORMING FOAM DRESSING?

CAVI-CARE CONFORMING FOAM DRESSING is a medical device that received FDA 510(k) clearance on 1994-08-19. The listed applicant is Smith & Nephew United, Inc.. The 510(k) number is K943619.

When did CAVI-CARE CONFORMING FOAM DRESSING receive FDA 510(k) clearance?

CAVI-CARE CONFORMING FOAM DRESSING received FDA 510(k) clearance on 1994-08-19, under 510(k) number K943619.

Who is the listed applicant for CAVI-CARE CONFORMING FOAM DRESSING?

The FDA 510(k) record lists Smith & Nephew United, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAVI-CARE CONFORMING FOAM DRESSING?

The FDA product code for CAVI-CARE CONFORMING FOAM DRESSING is KMF.

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Other records listing Smith & Nephew United, Inc. 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.

K963096ALLEVYN HYDRO POLY DRESSING ND ALL TRAC DRESSINGK961775PROFORE FOUR-LAYER BANDAGE SYSTEM KITK945330ALLEVYN ADHESIVEK942748INTRASITEK935705ALLEVYN ISLAND WOUND DRESSINGK935803CICA-CARE SILICONE GEL SHEET

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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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