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FDA 510(k)

KTI HY-Q(TM) WOUND DRESSING

K-Number: K940738 · 1994-05-06

ApplicantKingston Technologies, Inc.
Decision Date1994-05-06
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

KTI HY-Q(TM) WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Kingston Technologies, Inc.. It received FDA 510(k) clearance on 1994-05-06 under 510(k) number K940738. 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 KTI HY-Q(TM) WOUND DRESSING?

KTI HY-Q(TM) WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-05-06. The listed applicant is Kingston Technologies, Inc.. The 510(k) number is K940738.

When did KTI HY-Q(TM) WOUND DRESSING receive FDA 510(k) clearance?

KTI HY-Q(TM) WOUND DRESSING received FDA 510(k) clearance on 1994-05-06, under 510(k) number K940738.

Who is the listed applicant for KTI HY-Q(TM) WOUND DRESSING?

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

What is the FDA product code for KTI HY-Q(TM) WOUND DRESSING?

The FDA product code for KTI HY-Q(TM) WOUND DRESSING is KMF.

Related Clinical Trials

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Other records listing Kingston Technologies, 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.

K935232HYDROTORQUE GUIDE WIREK940814HYDRO-M(TM) WOUND GELK925660KTI TRANSPARENT WOUND DRESSINGK921502HYSORB WOUND DRESSINGK882157PANAMEX(TM) URETERAL STENT

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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