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SURGITEK ERECTEK TM EXTERNAL ERECTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K905015
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1990
Days to Decision
51 days

SURGITEK ERECTEK TM EXTERNAL ERECTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K905015
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1990
Days to Decision
51 days