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SURGITEK INFUSER

Page Type
Cleared 510(K)
510(k) Number
K941952
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1994
Days to Decision
32 days
Submission Type
Statement

SURGITEK INFUSER

Page Type
Cleared 510(K)
510(k) Number
K941952
510(k) Type
Traditional
Applicant
SURGITEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1994
Days to Decision
32 days
Submission Type
Statement