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PERITONEAL CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K902101
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1990
Days to Decision
80 days

PERITONEAL CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K902101
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1990
Days to Decision
80 days