Last synced on 10 January 2025 at 11:05 pm

ACUTRON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211000
510(k) Type
Traditional
Applicant
ILOODA Co., Ltd
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/9/2022
Days to Decision
433 days
Submission Type
Summary

ACUTRON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211000
510(k) Type
Traditional
Applicant
ILOODA Co., Ltd
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/9/2022
Days to Decision
433 days
Submission Type
Summary