Last synced on 30 September 2022 at 11:05 pm

VISUCAM PRO NM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052268
510(k) Type
Special
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2005
Days to Decision
75 days
Submission Type
Summary

VISUCAM PRO NM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052268
510(k) Type
Special
Applicant
CARL ZEISS MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2005
Days to Decision
75 days
Submission Type
Summary