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RENAK-E & RENEK-A SERIES HOLLOW FIBER DIALYZERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883748
510(k) Type
Traditional
Applicant
KAWASUMI LABORATORIES CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
1/31/1989
Days to Decision
152 days

RENAK-E & RENEK-A SERIES HOLLOW FIBER DIALYZERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883748
510(k) Type
Traditional
Applicant
KAWASUMI LABORATORIES CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
1/31/1989
Days to Decision
152 days