Last synced on 25 January 2026 at 3:41 am

RS-3000 ADVANCE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132323
510(k) Type
Traditional
Applicant
Nidek Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2014
Days to Decision
209 days
Submission Type
Summary

RS-3000 ADVANCE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132323
510(k) Type
Traditional
Applicant
Nidek Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2014
Days to Decision
209 days
Submission Type
Summary