Fiberoptic Sensor Technlogies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fiberoptic Sensor Technlogies, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Fiberoptic Sensor Technlogies, Inc. has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in Plymouth, US.
Historical record: 11 cleared submissions from 1987 to 1995.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fiberoptic Sensor Technlogies, Inc.
11 devices
Cleared
May 11, 1995
FST FIBEROPTIC PRESSURE CONVERTER
Gastroenterology & Urology
169d
Cleared
Apr 07, 1995
FST CATH-UD, CATHETER
Gastroenterology & Urology
50d
Cleared
Feb 09, 1995
4-CHANNEL URODYNAMIC MONITOR WITH URO-FLO OPTION
Gastroenterology & Urology
93d
Cleared
Nov 04, 1993
FST DUAL, DUAL PRESSURE URODYNAMICS MONITOR
Gastroenterology & Urology
295d
Cleared
Jul 20, 1993
URO-PRO 2000
Gastroenterology & Urology
420d
Cleared
Jul 20, 1993
FST COUNCIL TIP FOLEY CATHETER
Gastroenterology & Urology
406d
Cleared
Jun 18, 1993
FST CATH UD-DUAL DUAL PRESSURE CATHETER
Gastroenterology & Urology
198d
Cleared
Oct 09, 1991
FST CATH-UD CATHETER, MODIFICATION
Gastroenterology & Urology
96d
Cleared
Oct 08, 1991
FST CATH - UI USRODYNAMIC CATH INTRODUCER SYSTEM
Gastroenterology & Urology
49d
Cleared
Feb 19, 1991
FST CATH-UD CATHETER
Gastroenterology & Urology
63d
Cleared
Jan 16, 1987
FST DISPOSABLE FIBER OPTIC TRANSDUCER #0100-00
Cardiovascular
94d