Last synced on 25 January 2026 at 3:41 am

EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software Upgrade; EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software License

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223094
510(k) Type
Traditional
Applicant
Abbott Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2022
Days to Decision
88 days
Submission Type
Summary

EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software Upgrade; EnSite™ X EP System TactiFlex™ Ablation Catheter, Sensor Enabled™, Software License

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223094
510(k) Type
Traditional
Applicant
Abbott Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2022
Days to Decision
88 days
Submission Type
Summary