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URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071822
510(k) Type
Traditional
Applicant
UROPLASTY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2007
Days to Decision
48 days
Submission Type
Summary

URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071822
510(k) Type
Traditional
Applicant
UROPLASTY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2007
Days to Decision
48 days
Submission Type
Summary