Last synced on 14 November 2025 at 11:06 pm

ENDOLOGIX GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K110241
510(k) Type
Special
Applicant
TECHDEVICE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2011
Days to Decision
29 days
Submission Type
Summary

ENDOLOGIX GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K110241
510(k) Type
Special
Applicant
TECHDEVICE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2011
Days to Decision
29 days
Submission Type
Summary