Last synced on 25 January 2026 at 3:41 am

DIACLEAR ULTRAFILTER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003957
510(k) Type
Traditional
Applicant
Gambro Renal Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2001
Days to Decision
315 days
Submission Type
Statement

DIACLEAR ULTRAFILTER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003957
510(k) Type
Traditional
Applicant
Gambro Renal Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2001
Days to Decision
315 days
Submission Type
Statement