Conway Stuart Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conway Stuart Medical, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Conway Stuart Medical, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Sunnyvale, US.
Historical record: 10 cleared submissions from 1998 to 2000.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Conway Stuart Medical, Inc.
10 devices
Cleared
Apr 18, 2000
CSM STRETTA SYSTEM
General & Plastic Surgery
82d
Cleared
Feb 14, 2000
SECCA TUBULAR ELECTRODE DEVICE, MODEL A4000
General & Plastic Surgery
27d
Cleared
Oct 27, 1999
TUBULAR ELECTRODE DEVICE
General & Plastic Surgery
89d
Cleared
Sep 14, 1999
CSM STRETTA CONTROL MODULE ELECTROSURGICAL GENERATOR, MODEL S400
General & Plastic Surgery
134d
Cleared
Aug 13, 1999
CONWAY STUART MODEL 100 IRRIGATION PUMP & ACCESSORIES
General & Plastic Surgery
161d
Cleared
Jul 14, 1999
STRETTA INFLATABLE BASKET CATHETER ELECTRODE WITH ASPIRATION
General & Plastic Surgery
90d
Cleared
Mar 23, 1999
CONWAY STUART MEDICAL MODEL C4 ELECTROSURGICAL GENERATOR
General & Plastic Surgery
134d
Cleared
Dec 03, 1998
ELECTROSURGICAL INFLATABLE BASKET ELECTRODES
General & Plastic Surgery
90d
Cleared
Dec 01, 1998
DELIVERY SHEATH
Gastroenterology & Urology
63d
Cleared
Jul 30, 1998
ELECTROSURGICAL BASKET ELECTRODES...
General & Plastic Surgery
87d