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INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070217
510(k) Type
Traditional
Applicant
NEURO RESOURCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2008
Days to Decision
437 days
Submission Type
Summary

INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070217
510(k) Type
Traditional
Applicant
NEURO RESOURCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2008
Days to Decision
437 days
Submission Type
Summary