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SURGITEK ERECTEK TM EXTERNAL ERECTION DEVICE

Page Type
Cleared 510(K)
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)
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