Clk Intl., Inc. is one of 7103 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Clk Intl., Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 2 cleared submissions from 1998 to 1998. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Clk Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Clk Intl., Inc.
2 devices