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URESIL NEPHROSTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K923097
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1992
Days to Decision
81 days
Submission Type
Statement

URESIL NEPHROSTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K923097
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1992
Days to Decision
81 days
Submission Type
Statement