Last synced on 2 December 2022 at 11:04 pm

KERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112787
510(k) Type
Traditional
Applicant
KJ MEDITECH CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2012
Days to Decision
317 days
Submission Type
Summary

KERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112787
510(k) Type
Traditional
Applicant
KJ MEDITECH CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2012
Days to Decision
317 days
Submission Type
Summary