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Neurotron, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
6
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K853608
NEUROMETER
June 12, 1986
K843924
DIGITAL ELECTRONEUROMETER S-100
March 12, 1985