Last synced on 9 May 2025 at 11:05 pm

RESCAN 700

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233421
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/8/2024
Days to Decision
150 days
Submission Type
Summary

RESCAN 700

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233421
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/8/2024
Days to Decision
150 days
Submission Type
Summary