Curon Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curon Medical, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Curon Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 3 cleared submissions from 2000 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Curon Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Curon Medical, Inc.
3 devices
Cleared
Mar 21, 2002
SECCA SYSTEM
General & Plastic Surgery
90d
Cleared
Feb 21, 2001
CONTROL MODULE ALGORITHM ENHANCEMENT FOR THE MODEL S500-ST AND MODEL S400
General & Plastic Surgery
29d
Cleared
Oct 17, 2000
CURON CONTROL MODULE ELECTROSURGICAL GENERATOR AND ACCESSORIES, MODEL S500-ST
General & Plastic Surgery
29d