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Stoelting Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K012011
MODIFICATION TO A620 EEG
October 10, 2001
K965006
AT 62 EEG (A.K.A THE A;PHA-THETA TRAINER)
February 5, 1997
K952797
AT53 DUAL CHANNEL EMG
April 17, 1996
K944615
A620 EEG
September 18, 1995