Last synced on 9 May 2025 at 11:05 pm

Remex KA6

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212144
510(k) Type
Traditional
Applicant
Remedi Co. Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
8/3/2021
Days to Decision
25 days
Submission Type
Summary

Remex KA6

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212144
510(k) Type
Traditional
Applicant
Remedi Co. Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
8/3/2021
Days to Decision
25 days
Submission Type
Summary