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Revaclear 500, Revaclear 400, Revaclear 300

Page Type
Cleared 510(K)
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)
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