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Moda-flx Hemodialysis System and Cartridge

Page Type
Cleared 510(K)
510(k) Number
K233798
510(k) Type
Traditional
Applicant
Diality, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2024
Days to Decision
247 days
Submission Type
Summary

Moda-flx Hemodialysis System and Cartridge

Page Type
Cleared 510(K)
510(k) Number
K233798
510(k) Type
Traditional
Applicant
Diality, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2024
Days to Decision
247 days
Submission Type
Summary