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DUAL LUMEN L-CATH CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925979
510(k) Type
Traditional
Applicant
LUTHER MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1993
Days to Decision
183 days
Submission Type
Statement

DUAL LUMEN L-CATH CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925979
510(k) Type
Traditional
Applicant
LUTHER MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1993
Days to Decision
183 days
Submission Type
Statement