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NIPRO PUREFLUX-L HEMODIALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122952
510(k) Type
Traditional
Applicant
NIPRO MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2013
Days to Decision
435 days
Submission Type
Summary

NIPRO PUREFLUX-L HEMODIALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122952
510(k) Type
Traditional
Applicant
NIPRO MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2013
Days to Decision
435 days
Submission Type
Summary