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DANTEC MAGLITE MAGNETIC STIMULATOR (MAGLITE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931923
510(k) Type
Traditional
Applicant
DANTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1993
Days to Decision
207 days
Submission Type
Summary

DANTEC MAGLITE MAGNETIC STIMULATOR (MAGLITE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931923
510(k) Type
Traditional
Applicant
DANTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1993
Days to Decision
207 days
Submission Type
Summary