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MYOTouch Muscle Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233098
510(k) Type
Traditional
Applicant
SunMed LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2024
Days to Decision
311 days
Submission Type
Summary

MYOTouch Muscle Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233098
510(k) Type
Traditional
Applicant
SunMed LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2024
Days to Decision
311 days
Submission Type
Summary