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CATHETER INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K924562
510(k) Type
Traditional
Applicant
LUTHER MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1993
Days to Decision
169 days
Submission Type
Statement

CATHETER INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K924562
510(k) Type
Traditional
Applicant
LUTHER MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1993
Days to Decision
169 days
Submission Type
Statement