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Finetone Hearing Instruments

FDA Regulatory Profile

Finetone Hearing Instruments appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 20, 1998.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K974219FACEPLATE ASSEMBLYFebruary 20, 1998
K955692FINETONE FSC,February 2, 1996
K945780FINETONE DISCEET CANALDecember 21, 1994
K940164SUPER-SILJune 29, 1994
K830960CUSTOM IN-THE-EAR HEARING AIDJune 30, 1983

FDA data resources