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URESIL ENDOSCOPIC LASER OVERTUBE

Page Type
Cleared 510(K)
510(k) Number
K901882
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1990
Days to Decision
92 days

URESIL ENDOSCOPIC LASER OVERTUBE

Page Type
Cleared 510(K)
510(k) Number
K901882
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1990
Days to Decision
92 days