Last synced on 9 December 2022 at 11:04 pm

PRISMAFLEX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110823
510(k) Type
Traditional
Applicant
GAMBRO RENAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2011
Days to Decision
85 days
Submission Type
Summary

PRISMAFLEX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110823
510(k) Type
Traditional
Applicant
GAMBRO RENAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2011
Days to Decision
85 days
Submission Type
Summary