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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
K222079
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2022
Days to Decision
88 days
Submission Type
Summary