Last synced on 22 September 2023 at 11:04 pm

CORE-INJECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221054
510(k) Type
Traditional
Applicant
Incore Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/21/2022
Days to Decision
254 days
Submission Type
Summary

CORE-INJECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221054
510(k) Type
Traditional
Applicant
Incore Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/21/2022
Days to Decision
254 days
Submission Type
Summary