Last synced on 12 July 2024 at 11:04 pm

Slinky Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231179
510(k) Type
Traditional
Applicant
Anoxia Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
219 days
Submission Type
Summary

Slinky Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231179
510(k) Type
Traditional
Applicant
Anoxia Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
219 days
Submission Type
Summary