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IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024100
510(k) Type
Traditional
Applicant
THERATECH, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
2/25/2003
Days to Decision
75 days
Submission Type
Summary

IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024100
510(k) Type
Traditional
Applicant
THERATECH, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
2/25/2003
Days to Decision
75 days
Submission Type
Summary