Last synced on 14 June 2024 at 11:05 pm

VPC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190345
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/16/2019
Days to Decision
91 days
Submission Type
Summary

VPC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190345
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/16/2019
Days to Decision
91 days
Submission Type
Summary