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SINGLE LUMEN CATHETER KITS

Page Type
Cleared 510(K)
510(k) Number
K904139
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
12/4/1990
Days to Decision
89 days

SINGLE LUMEN CATHETER KITS

Page Type
Cleared 510(K)
510(k) Number
K904139
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
12/4/1990
Days to Decision
89 days