FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

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

K Number: K254014 · Decision Jan 13, 2026
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
101
Review Days
29

Basic Information

Device Name
Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control
K Number
K254014
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
December 15, 2025
Decision Date
January 13, 2026
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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