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ALEVE Direct Therapy (ALEVE Direct Therapy TENS Device)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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