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FDA 510(k)

HYDRON WOUND DRESSING KIT

K-Number: K811446 · 1981-06-12

ApplicantNational Patent Development Corp.
Decision Date1981-06-12
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYDRON WOUND DRESSING KIT is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1981-06-12 under 510(k) number K811446. 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 HYDRON WOUND DRESSING KIT?

HYDRON WOUND DRESSING KIT is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is National Patent Development Corp.. The 510(k) number is K811446.

When did HYDRON WOUND DRESSING KIT receive FDA 510(k) clearance?

HYDRON WOUND DRESSING KIT received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811446.

Who is the listed applicant for HYDRON WOUND DRESSING KIT?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDRON WOUND DRESSING KIT?

The FDA product code for HYDRON WOUND DRESSING KIT is KMF.

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Other records listing National Patent Development Corp. 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.

K843974VARIABLE TEMPERATURE CAUTERY DEVICEK832699HYDRON WOUND DRESSING FAST SEAT KITK822793PIO ROOT CANAL INDICATORK820028ZEON COMPOSITE RESIN LIGHT CURE SYSK820006ZEON COMPOSITE RESIN SYSTEMK801482HYDRON ROOT CANAL FILLING MATERIAL

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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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