Last synced on 20 December 2024 at 11:05 pm

ICEfx Cryoablation System (FPRCH8000-02)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234002
510(k) Type
Traditional
Applicant
Boston Scientific
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2024
Days to Decision
85 days
Submission Type
Summary

ICEfx Cryoablation System (FPRCH8000-02)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234002
510(k) Type
Traditional
Applicant
Boston Scientific
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2024
Days to Decision
85 days
Submission Type
Summary