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REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050046
510(k) Type
Traditional
Applicant
COMPEX TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2005
Days to Decision
93 days
Submission Type
Summary

REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050046
510(k) Type
Traditional
Applicant
COMPEX TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2005
Days to Decision
93 days
Submission Type
Summary