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OCCLUSIN 500 ARTIFICIAL EMBOLIZATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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