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INTRAVASCULAR CATHETER SECURMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K912211
510(k) Type
Traditional
Applicant
INMAN LIEBELT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1991
Days to Decision
81 days
Submission Type
Statement

INTRAVASCULAR CATHETER SECURMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K912211
510(k) Type
Traditional
Applicant
INMAN LIEBELT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1991
Days to Decision
81 days
Submission Type
Statement