The following data is part of a premarket notification filed by Fiberoptic Sensor Technlogies, Inc. with the FDA for Fst Dual, Dual Pressure Urodynamics Monitor.
Device ID | K930171 |
510k Number | K930171 |
Device Name: | FST DUAL, DUAL PRESSURE URODYNAMICS MONITOR |
Classification | Device, Cystometric, Hydraulic |
Applicant | FIBEROPTIC SENSOR TECHNLOGIES, INC. 501 AVIS DR. Ann Arbor, MI 48108 |
Contact | Douglas G Tomasko |
Correspondent | Douglas G Tomasko FIBEROPTIC SENSOR TECHNLOGIES, INC. 501 AVIS DR. Ann Arbor, MI 48108 |
Product Code | FEN |
CFR Regulation Number | 876.1620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-01-13 |
Decision Date | 1993-11-04 |