Last synced on 6 June 2025 at 11:06 pm

MODIFIED ACUMEN LEAD DELIVERY SHEATH, MODELS LDS-10-57, LDS-10-57-90, LDS-10-64 AND LDS-10-64-90

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062145
510(k) Type
Special
Applicant
ACUMEN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2006
Days to Decision
27 days
Submission Type
Summary

MODIFIED ACUMEN LEAD DELIVERY SHEATH, MODELS LDS-10-57, LDS-10-57-90, LDS-10-64 AND LDS-10-64-90

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062145
510(k) Type
Special
Applicant
ACUMEN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2006
Days to Decision
27 days
Submission Type
Summary