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LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912165
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
12/11/1991
Days to Decision
209 days
Submission Type
Statement

LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912165
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
12/11/1991
Days to Decision
209 days
Submission Type
Statement