Last synced on 25 April 2025 at 11:05 pm

AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL10060060

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041374
510(k) Type
Traditional
Applicant
IDEV TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2005
Days to Decision
282 days
Submission Type
Summary

AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL10060060

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041374
510(k) Type
Traditional
Applicant
IDEV TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2005
Days to Decision
282 days
Submission Type
Summary