Last synced on 25 November 2022 at 11:04 pm

Revaclear 500, Revaclear 400, Revaclear 300

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213639
510(k) Type
Traditional
Applicant
Baxter Healthcare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2022
Days to Decision
67 days
Submission Type
Summary

Revaclear 500, Revaclear 400, Revaclear 300

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213639
510(k) Type
Traditional
Applicant
Baxter Healthcare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2022
Days to Decision
67 days
Submission Type
Summary