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AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071120
510(k) Type
Traditional
Applicant
Aemed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2008
Days to Decision
328 days
Submission Type
Summary

AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071120
510(k) Type
Traditional
Applicant
Aemed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2008
Days to Decision
328 days
Submission Type
Summary