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VERESS CANNULA AND MODULAR VERESS CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062097
510(k) Type
Traditional
Applicant
PAJUNK GMBH MEDIZINTECHNOLOGIE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/13/2006
Days to Decision
81 days
Submission Type
Summary

VERESS CANNULA AND MODULAR VERESS CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062097
510(k) Type
Traditional
Applicant
PAJUNK GMBH MEDIZINTECHNOLOGIE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/13/2006
Days to Decision
81 days
Submission Type
Summary