KTI TRANSPARENT WOUND DRESSING— 510(k) K925660

Name: FDA 510(k) clearance K925660
Creator: U.S. Food and Drug Administration
Published: 1993-04-20

Substantially Equivalent

Kingston Technologies, Inc.

FDA 510(k) clearance K925660 for KTI TRANSPARENT WOUND DRESSING, Substantially Equivalent on 1993-04-20. Applicant: Kingston Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Kingston Technologies, Inc.
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-11-10
Decision date: 1993-04-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dayton, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MGP

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K012995 — COLLATEK SHEET2001-10-25
K012997 — COLLATEK FOAM2001-10-25
K001508 — LASERSKIN DRESSING2001-07-25
K990079 — FASTSEAL CHEST WOUND DRESSING1999-12-23
K991214 — SIMPLICARE TRANSPARENT WOUND DRESSING1999-10-14

More clearances from Kingston Technologies, Inc.

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K935232 — HYDROTORQUE GUIDE WIRE1994-07-20
K940814 — HYDRO-M(TM) WOUND GEL1994-05-12
K940738 — KTI HY-Q(TM) WOUND DRESSING1994-05-06
K921502 — HYSORB WOUND DRESSING1992-09-29
K882157 — PANAMEX(TM) URETERAL STENT1988-08-02

Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.