Last synced on 14 November 2025 at 11:06 pm

ACUTRON

Page Type
Cleared 510(K)
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)
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