Kingston Technologies, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kingston Technologies, Inc. General & Plastic Surgery ✕
4 devices
Cleared
May 12, 1994
HYDRO-M(TM) WOUND GEL
General & Plastic Surgery
79d
Cleared
May 06, 1994
KTI HY-Q(TM) WOUND DRESSING
General & Plastic Surgery
78d
Cleared
Apr 20, 1993
KTI TRANSPARENT WOUND DRESSING
General & Plastic Surgery
161d
Cleared
Sep 29, 1992
HYSORB WOUND DRESSING
General & Plastic Surgery
182d