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FDA 510(k)

ALLCLENZ WOUND CLEANSER

K-Number: K965120 · 1997-03-21

ApplicantDpt Laboratories, Ltd.
Decision Date1997-03-21
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

ALLCLENZ WOUND CLEANSER is the device name listed in this FDA 510(k) record. The listed applicant is Dpt Laboratories, Ltd.. It received FDA 510(k) clearance on 1997-03-21 under 510(k) number K965120. 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 ALLCLENZ WOUND CLEANSER?

ALLCLENZ WOUND CLEANSER is a medical device that received FDA 510(k) clearance on 1997-03-21. The listed applicant is Dpt Laboratories, Ltd.. The 510(k) number is K965120.

When did ALLCLENZ WOUND CLEANSER receive FDA 510(k) clearance?

ALLCLENZ WOUND CLEANSER received FDA 510(k) clearance on 1997-03-21, under 510(k) number K965120.

Who is the listed applicant for ALLCLENZ WOUND CLEANSER?

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

What is the FDA product code for ALLCLENZ WOUND CLEANSER?

The FDA product code for ALLCLENZ WOUND CLEANSER is KMF.

Related Clinical Trials

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Other records listing Dpt Laboratories, Ltd. 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.

K953816DCURASOL GEL WOUND DRESSINGK953450CURASOL GEL 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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