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FDA 510(k)

KTI TRANSPARENT WOUND DRESSING

K-Number: K925660 · 1993-04-20

ApplicantKingston Technologies, Inc.
Decision Date1993-04-20
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

KTI TRANSPARENT 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 1993-04-20 under 510(k) number K925660. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KTI TRANSPARENT WOUND DRESSING?

KTI TRANSPARENT WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Kingston Technologies, Inc.. The 510(k) number is K925660.

When did KTI TRANSPARENT WOUND DRESSING receive FDA 510(k) clearance?

KTI TRANSPARENT WOUND DRESSING received FDA 510(k) clearance on 1993-04-20, under 510(k) number K925660.

Who is the listed applicant for KTI TRANSPARENT 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 TRANSPARENT WOUND DRESSING?

The FDA product code for KTI TRANSPARENT WOUND DRESSING is MGP.

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 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 GELK940738KTI HY-Q(TM) WOUND DRESSINGK921502HYSORB WOUND DRESSINGK882157PANAMEX(TM) URETERAL STENT

Related Devices (Code: MGP)

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.

K012995COLLATEK SHEETBiocore Medical Technologies, Inc.K012997COLLATEK FOAMBiocore Medical Technologies, Inc.K001508LASERSKIN DRESSINGFidia Advanced Biopolymers SrlK990079FASTSEAL CHEST WOUND DRESSINGGreenfield Medical Technologies, Inc.K991214SIMPLICARE TRANSPARENT WOUND DRESSINGHollister, Inc.K992302DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORSDermaphylyx, 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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