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URESIL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K942191
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1994
Days to Decision
140 days
Submission Type
Statement

URESIL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K942191
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1994
Days to Decision
140 days
Submission Type
Statement