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CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033358
510(k) Type
Traditional
Applicant
SURGITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2003
Days to Decision
25 days
Submission Type
Summary

CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033358
510(k) Type
Traditional
Applicant
SURGITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2003
Days to Decision
25 days
Submission Type
Summary