Kingston Technologies, Inc.

6 FDA 510(k) medical device clearances.

Top product codes for Kingston Technologies, Inc.

KMF — General Hospital 2 devices
DQX — Cardiovascular 1 device
FAD — Gastroenterology, Urology 1 device
MGP — Unknown 1 device
MGQ — Unknown 1 device

Recent clearances by Kingston Technologies, Inc.

K935232 — HYDROTORQUE GUIDE WIRE DQX · 1994-07-20
K940814 — HYDRO-M(TM) WOUND GEL MGQ · 1994-05-12
K940738 — KTI HY-Q(TM) WOUND DRESSING KMF · 1994-05-06
K925660 — KTI TRANSPARENT WOUND DRESSING MGP · 1993-04-20
K921502 — HYSORB WOUND DRESSING KMF · 1992-09-29
K882157 — PANAMEX(TM) URETERAL STENT FAD · 1988-08-02

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