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FDA 510(k)

CUTINOVA THIN WOUND DRESSING

K-Number: K944581 · 1994-12-02

ApplicantBeiersdorf, Inc.
Decision Date1994-12-02
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

CUTINOVA THIN WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1994-12-02 under 510(k) number K944581. 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 CUTINOVA THIN WOUND DRESSING?

CUTINOVA THIN WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-12-02. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K944581.

When did CUTINOVA THIN WOUND DRESSING receive FDA 510(k) clearance?

CUTINOVA THIN WOUND DRESSING received FDA 510(k) clearance on 1994-12-02, under 510(k) number K944581.

Who is the listed applicant for CUTINOVA THIN WOUND DRESSING?

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

What is the FDA product code for CUTINOVA THIN WOUND DRESSING?

The FDA product code for CUTINOVA THIN WOUND DRESSING is KMF.

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Other records listing Beiersdorf, 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.

K090921ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02K024057CURAD SCAR THERAPYK952526CUTINOVA CAVITYK943363CUTIPLAST STERILK935630NORTAK940378COVERLET ADHESIVE DRESSING

View all 45 devices →

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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