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CP Relief Wand-OTC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162630
510(k) Type
Traditional
Applicant
Mid-America Medical Innovations LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2016
Days to Decision
90 days
Submission Type
Summary

CP Relief Wand-OTC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162630
510(k) Type
Traditional
Applicant
Mid-America Medical Innovations LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2016
Days to Decision
90 days
Submission Type
Summary