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Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230886
510(k) Type
Special
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2023
Days to Decision
82 days
Submission Type
Summary