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/ The Telos Co.
The Telos Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K812778
THE TELOS EQUIPMENT
December 8, 1981
K812779
EXTENSIONS-LUSATZTISCH
October 26, 1981