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OCCLUSIN 500 ARTIFICIAL EMBOLIZATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093813
510(k) Type
Traditional
Applicant
IMBIOTECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2010
Days to Decision
150 days
Submission Type
Summary

OCCLUSIN 500 ARTIFICIAL EMBOLIZATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093813
510(k) Type
Traditional
Applicant
IMBIOTECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2010
Days to Decision
150 days
Submission Type
Summary