C&H International is one of 25749 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
C&H International - FDA 510(k) Cleared Devices
Recent clearances: TDP HEAT LAMP OR INFRARED HEATING LAMP, MODELS CQG-S1, CQG-111A/B, CQG-222A/B, CQG-270A/B, CQG-222D
1
Total
1
Cleared
0
Denied
C&H International has 1 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by C&H International Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - C&H International
1 devices