KTI HY-Q(TM) WOUND DRESSING— 510(k) K940738

Name: FDA 510(k) clearance K940738
Creator: U.S. Food and Drug Administration
Published: 1994-05-06

Substantially Equivalent for Some Indications

Kingston Technologies, Inc.

FDA 510(k) clearance K940738 for KTI HY-Q(TM) WOUND DRESSING, Substantially Equivalent for Some Indications on 1994-05-06. Applicant: Kingston Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Kingston Technologies, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1994-02-17
Decision date: 1994-05-06
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Dayton, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMF

view all

K241916 — TearRepair Liquid Skin Protectant2024-09-27
K182733 — Rochal Bioshield Silicone Film2019-06-27
K171148 — Aleo BME Liquid Bandage2018-01-12
K153571 — Cavilon Advanced High Endurance Skin Protectant2016-08-23
K160684 — Atteris No-Sting Skin Protectant2016-07-26

More clearances from Kingston Technologies, Inc.

view all

K935232 — HYDROTORQUE GUIDE WIRE1994-07-20
K940814 — HYDRO-M(TM) WOUND GEL1994-05-12
K925660 — KTI TRANSPARENT WOUND DRESSING1993-04-20
K921502 — HYSORB WOUND DRESSING1992-09-29
K882157 — PANAMEX(TM) URETERAL STENT1988-08-02

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