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DUO-FLUX(R) ULTRA HIGH PERFORM ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913950
510(k) Type
Traditional
Applicant
ALTHIN MEDICAL AB AN AFFILIATE OF BAXTER INTL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1991
Days to Decision
58 days
Submission Type
Statement

DUO-FLUX(R) ULTRA HIGH PERFORM ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913950
510(k) Type
Traditional
Applicant
ALTHIN MEDICAL AB AN AFFILIATE OF BAXTER INTL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1991
Days to Decision
58 days
Submission Type
Statement