Exos, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
0
Compliance Actions
0

Known Names

exos, exo-s

Recent 510(k) Clearances

K-NumberDeviceDate
K922940CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002October 5, 1992