Last synced on 19 July 2024 at 11:05 pm

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
K152852
510(k) Type
Traditional
Applicant
BAYER HEALTHCARE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2015
Days to Decision
84 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
K152852
510(k) Type
Traditional
Applicant
BAYER HEALTHCARE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2015
Days to Decision
84 days
Submission Type
Summary