Synectics-Dantec - FDA 510(k) Cleared Devices
19
Total
18
Cleared
0
Denied
Synectics-Dantec has 18 FDA 510(k) cleared gastroenterology & urology devices. Based in Chicago, US.
Historical record: 18 cleared submissions from 1985 to 1997.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Jan 29, 1997
PH ANALYSIS MODULE
Gastroenterology & Urology
320d
Cleared
Sep 30, 1994
ZINETICS COMPOSITE SENSOR PROBE W/INTERNAL REF.
Gastroenterology & Urology
704d
Cleared
Jun 30, 1994
MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS
Anesthesiology
654d
Cleared
Dec 13, 1993
MONOCRYSTANT PH/LES CATHETER, MODIFICATION
Gastroenterology & Urology
840d
Cleared
Jun 18, 1993
SYNECTICS LIBERTY SYSTEM, PC POLYGRAF/POLYGRAM URO
Gastroenterology & Urology
297d
Cleared
Jun 11, 1992
MONOCRYSTANT PH-REFERENCE CATHETER, MODIFICATION
Gastroenterology & Urology
290d
Cleared
Apr 28, 1992
PH METER, MODIFICATION
Gastroenterology & Urology
195d
Cleared
Feb 26, 1992
AIRWAY THERMISTOR
Anesthesiology
160d
Cleared
Dec 27, 1991
DIGITRAPPER MARK III
Gastroenterology & Urology
151d
Cleared
Aug 20, 1991
SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM
Anesthesiology
314d
Cleared
Apr 26, 1991
MICROTRAPPER/MICRODIGITRAPPER, MODIFICATION
Anesthesiology
140d
Cleared
Jun 11, 1990
SYNECTICS LIBERTY SYSTEM, PC POLYGRAF & POLYGRAM
Gastroenterology & Urology
129d