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FDA 510(k)

MULTIDEX HYDROPHILIC WOUND DRESSING

K-Number: K945000 · 1994-11-17

ApplicantLange Medical Products, Inc.
Decision Date1994-11-17
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTIDEX 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 1994-11-17 under 510(k) number K945000. 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 HYDROPHILIC WOUND DRESSING?

MULTIDEX HYDROPHILIC WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-11-17. The listed applicant is Lange Medical Products, Inc.. The 510(k) number is K945000.

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

MULTIDEX HYDROPHILIC WOUND DRESSING received FDA 510(k) clearance on 1994-11-17, under 510(k) number K945000.

Who is the listed applicant for MULTIDEX 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 HYDROPHILIC WOUND DRESSING?

The FDA product code for MULTIDEX 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 GELK955399MULTIDEX PLUS HYDROPHILIC WOUND DRESSINGK952774MULTIDEX GEL

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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