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RADIANCE ULTRA 32 4K ZEROWIRE DUO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222890
510(k) Type
Special
Applicant
NDS Surgical Imaging, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2022
Days to Decision
26 days
Submission Type
Summary