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FDA 510(k)

CUTINOVA CAVITY

K-Number: K952526 · 1995-08-14

ApplicantBeiersdorf, Inc.
Decision Date1995-08-14
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

CUTINOVA CAVITY is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1995-08-14 under 510(k) number K952526. 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 CAVITY?

CUTINOVA CAVITY is a medical device that received FDA 510(k) clearance on 1995-08-14. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K952526.

When did CUTINOVA CAVITY receive FDA 510(k) clearance?

CUTINOVA CAVITY received FDA 510(k) clearance on 1995-08-14, under 510(k) number K952526.

Who is the listed applicant for CUTINOVA CAVITY?

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 CAVITY?

The FDA product code for CUTINOVA CAVITY 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 THERAPYK943363CUTIPLAST STERILK944581CUTINOVA THIN WOUND DRESSINGK935630NORTAK940378COVERLET ADHESIVE 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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