# Fiberoptic Sensor Technlogies, Inc.

- Location (FDA's records): Ann Arbor, MI
- FDA decisions: 11 (1987–1995): 11 510(k) clearances
- Product codes: FEN (8), EXY (1), FAP (1), DXO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K945753: FST Fiberoptic Pressure Converter (May 11, 1995)
- K950908: FST Cath-UD, Catheter (Apr 7, 1995)
- K945495: 4-Channel Urodynamic Monitor with Uro-Flo Option (Feb 9, 1995)
- K930171: FST Dual, Dual Pressure Urodynamics Monitor (Nov 4, 1993)
- K922476: Uro-Pro 2000 (Jul 20, 1993)
- K922776: FST Council Tip Foley Catheter (Jul 20, 1993)
- K926088: FST Cath UD-Dual Dual Pressure Catheter (Jun 18, 1993)
- K913113: FST Cath-UD Catheter, Modification (Oct 9, 1991)

Source page: https://510kreport.com/company/fiberoptic-sensor-technlogies