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SILITEK URINARY DIVERSION STENT

Page Type
Cleared 510(K)
510(k) Number
K840059
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1984
Days to Decision
26 days

SILITEK URINARY DIVERSION STENT

Page Type
Cleared 510(K)
510(k) Number
K840059
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1984
Days to Decision
26 days