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GAMBRO POLYFLUX HEMODIALYZER, MODEL 6H

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051520
510(k) Type
Traditional
Applicant
GAMBRO RENAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
184 days
Submission Type
Summary

GAMBRO POLYFLUX HEMODIALYZER, MODEL 6H

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051520
510(k) Type
Traditional
Applicant
GAMBRO RENAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
184 days
Submission Type
Summary