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FDA 510(k)

MULTIDEX PLUS HYDROPHILIC WOUND DRESSING

K-Number: K955399 · 1996-02-07

ApplicantLange Medical Products, Inc.
Decision Date1996-02-07
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTIDEX PLUS HYDROPHILIC WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Lange Medical Products, Inc.. It received FDA 510(k) clearance on 1996-02-07 under 510(k) number K955399. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIDEX PLUS HYDROPHILIC WOUND DRESSING?

MULTIDEX PLUS HYDROPHILIC WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1996-02-07. The listed applicant is Lange Medical Products, Inc.. The 510(k) number is K955399.

When did MULTIDEX PLUS HYDROPHILIC WOUND DRESSING receive FDA 510(k) clearance?

MULTIDEX PLUS HYDROPHILIC WOUND DRESSING received FDA 510(k) clearance on 1996-02-07, under 510(k) number K955399.

Who is the listed applicant for MULTIDEX PLUS HYDROPHILIC WOUND DRESSING?

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

What is the FDA product code for MULTIDEX PLUS HYDROPHILIC WOUND DRESSING?

The FDA product code for MULTIDEX PLUS HYDROPHILIC WOUND DRESSING is KMF.

Related Clinical Trials

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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Other records listing Lange Medical Products, 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.

K962917MULTIDEX HYDROPHILIC WOUND DRESSING GELK952774MULTIDEX GELK945000MULTIDEX HYDROPHILIC WOUND DRESSING

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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