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VERESS CANNULA AND MODULAR VERESS CANNULA

Page Type
Cleared 510(K)
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)
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