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INNOPORT LAPAROSCOPIC ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090677
510(k) Type
Traditional
Applicant
INNOVIA LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2009
Days to Decision
52 days
Submission Type
Summary

INNOPORT LAPAROSCOPIC ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090677
510(k) Type
Traditional
Applicant
INNOVIA LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2009
Days to Decision
52 days
Submission Type
Summary