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Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190663
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/17/2019
Days to Decision
94 days
Submission Type
Summary

Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190663
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/17/2019
Days to Decision
94 days
Submission Type
Summary