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C3 EXTERNAL MALE BLADDER CONTROL DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974040
510(k) Type
Traditional
Applicant
Timm Research Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1998
Days to Decision
263 days
Submission Type
Summary

C3 EXTERNAL MALE BLADDER CONTROL DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974040
510(k) Type
Traditional
Applicant
Timm Research Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1998
Days to Decision
263 days
Submission Type
Summary