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SINGLE LUMEN CATHETERS, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K904140
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1990
Days to Decision
82 days

SINGLE LUMEN CATHETERS, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K904140
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1990
Days to Decision
82 days