Clk Intl., Inc. - FDA 510(k) Cleared Devices
Recent clearances: CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE, CLK INT'L. SANITARY LATEX PROBE COVER, CLK ULTRASOUND PROBE COVER
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Clk Intl., Inc. General Hospital ✕
1 devices