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TENCKHOFF PERITONEAL DIALYSIS KIT

Page Type
Cleared 510(K)
510(k) Number
K902203
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
8/1/1990
Days to Decision
77 days

TENCKHOFF PERITONEAL DIALYSIS KIT

Page Type
Cleared 510(K)
510(k) Number
K902203
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
8/1/1990
Days to Decision
77 days