Fiberoptic Sensor Technlogies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K945753FST FIBEROPTIC PRESSURE CONVERTERMay 11, 1995
K950908FST CATH-UD, CATHETERApril 7, 1995
K9454954-CHANNEL URODYNAMIC MONITOR WITH URO-FLO OPTIONFebruary 9, 1995
K930171FST DUAL, DUAL PRESSURE URODYNAMICS MONITORNovember 4, 1993
K922476URO-PRO 2000July 20, 1993
K922776FST COUNCIL TIP FOLEY CATHETERJuly 20, 1993
K926088FST CATH UD-DUAL DUAL PRESSURE CATHETERJune 18, 1993
K913113FST CATH-UD CATHETER, MODIFICATIONOctober 9, 1991
K913721FST CATH - UI USRODYNAMIC CATH INTRODUCER SYSTEMOctober 8, 1991
K905641FST CATH-UD CATHETERFebruary 19, 1991
K864000FST DISPOSABLE FIBER OPTIC TRANSDUCER #0100-00January 16, 1987