Last synced on 23 February 2024 at 11:04 pm

ReFlow System Mini

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221918
510(k) Type
Traditional
Applicant
Anuncia Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2022
Days to Decision
90 days
Submission Type
Summary

ReFlow System Mini

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221918
510(k) Type
Traditional
Applicant
Anuncia Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2022
Days to Decision
90 days
Submission Type
Summary