Stellartech Research Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stellartech Research Corp. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Stellartech Research Corp. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Sunnyvale, US.
Historical record: 11 cleared submissions from 2000 to 2006.
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 - Stellartech Research Corp.
11 devices
Cleared
Oct 13, 2006
STELLARTECH 100 COAGULATION SYSTEM
General & Plastic Surgery
130d
Cleared
Apr 12, 2005
STELLARTECH COAGULATION SYSTEM 2, MODELS 1100C-115A AND 1100C-230A
General & Plastic Surgery
11d
Cleared
Nov 12, 2004
STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115A & 1100C-230A
General & Plastic Surgery
22d
Cleared
Jun 14, 2004
STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 AND 1100C-230
General & Plastic Surgery
20d
Cleared
Apr 01, 2004
STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)
General & Plastic Surgery
58d
Cleared
Oct 06, 2003
MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)
General & Plastic Surgery
33d
Cleared
Aug 21, 2003
MODIFICATION TO: STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 & 100C-230
General & Plastic Surgery
10d
Cleared
Jul 29, 2003
STELLARTECH COAGULATION SYSTEM, MODELS (1100C-115 & 1100C-230)
General & Plastic Surgery
26d
Cleared
Nov 29, 2002
STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)
General & Plastic Surgery
17d
Cleared
Dec 18, 2001
STELLARTECH COAGULATION SYSTEM
General & Plastic Surgery
90d
Cleared
Jan 20, 2000
STELLARTECH RADIOFREQUENCY GENERATOR,MODEL 1025A-115, STELLARTECH...
General & Plastic Surgery
41d