Last synced on 30 May 2025 at 11:05 pm

PeriCross™ Epicardial Access Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243954
510(k) Type
Traditional
Applicant
CIRCA Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2025
Days to Decision
122 days
Submission Type
Summary

PeriCross™ Epicardial Access Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243954
510(k) Type
Traditional
Applicant
CIRCA Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2025
Days to Decision
122 days
Submission Type
Summary