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ALEVE Direct Therapy (ALEVE Direct Therapy TENS Device)

Page Type
Cleared 510(K)
510(k) Number
K171802
510(k) Type
Traditional
Applicant
Bayer HealthCare LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2018
Days to Decision
261 days
Submission Type
Summary

ALEVE Direct Therapy (ALEVE Direct Therapy TENS Device)

Page Type
Cleared 510(K)
510(k) Number
K171802
510(k) Type
Traditional
Applicant
Bayer HealthCare LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2018
Days to Decision
261 days
Submission Type
Summary