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LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040550
510(k) Type
Special
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/16/2004
Days to Decision
14 days
Submission Type
Summary

LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040550
510(k) Type
Special
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
3/16/2004
Days to Decision
14 days
Submission Type
Summary