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MICROSTIM 100I TENS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K010295
510(k) Type
Traditional
Applicant
MICROSTIM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2001
Days to Decision
184 days
Submission Type
Summary

MICROSTIM 100I TENS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K010295
510(k) Type
Traditional
Applicant
MICROSTIM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2001
Days to Decision
184 days
Submission Type
Summary