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EROS-CLITORAL THERAPY DEVICE (CTD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN000006
510(k) Type
Post-NSE
Applicant
UROMETRICS, INC.
Country
United States
FDA Decision
Deleted
Decision Date
4/28/2000
Days to Decision
1 days

EROS-CLITORAL THERAPY DEVICE (CTD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN000006
510(k) Type
Post-NSE
Applicant
UROMETRICS, INC.
Country
United States
FDA Decision
Deleted
Decision Date
4/28/2000
Days to Decision
1 days