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URESIL SUBCLAVIAN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K863684
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1987
Days to Decision
109 days

URESIL SUBCLAVIAN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K863684
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1987
Days to Decision
109 days