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SURGITEK URINARY DIVERSION STENT

Page Type
Cleared 510(K)
510(k) Number
K800109
510(k) Type
Traditional
Applicant
MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1980
Days to Decision
41 days

SURGITEK URINARY DIVERSION STENT

Page Type
Cleared 510(K)
510(k) Number
K800109
510(k) Type
Traditional
Applicant
MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1980
Days to Decision
41 days