Last synced on 14 November 2025 at 11:06 pm

7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K880776
510(k) Type
Traditional
Applicant
MEDSURG INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1988
Days to Decision
66 days

7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K880776
510(k) Type
Traditional
Applicant
MEDSURG INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1988
Days to Decision
66 days