FDA device listing

12L-RS,12S-RS,3Sc-RS,4C-RS,6S-RS,6Tc-RS,8C-RS,9L-RS,9T-RS,C1-5-RS (only for Vivid T9),E8C-RS,E8Cs-RS (only for Vivid…

FDA device listing 1745719114 · GE HealthCare Technologies Inc.

Key facts

Proprietary names 12L-RS,12S-RS,3Sc-RS,4C-RS,6S-RS,6Tc-RS,8C-RS,9L-RS,9T-RS,C1-5-RS (only for Vivid T9),E8C-RS,E8Cs-RS (only for Vivid T9),L6-12-RS,L8-18i-RS,P2D,Vivid T8,Vivid T9
Owner/operator GE HealthCare Technologies Inc.
Owner/operator number 9912004
Premarket submissions K181934
Product codes ITX, IYN, IYO
Device names ITX - Transducer, Ultrasonic, Diagnostic, IYN - System, Imaging, Pulsed Doppler, Ultrasonic, IYO - System, Imaging, Pulsed Echo, Ultrasonic
Device class Class II
Classification regulations (21 CFR) 892.1550, 892.1560, 892.1570
Review panels Radiology
Registered establishments GE Healthcare Japan Corporation, GE MEDICAL SYSTEMS (CHINA) CO., LTD., GE PARALLEL DESIGN, INC., GE VINGMED ULTRASOUND A/S, PARALLEL DESIGN SAS, Wipro GE Healthcare Private Ltd., WIPRO GE MEDICAL DEVICE MANUFACTURING PRIVATE LIMITED
Establishment registrations 2032350, 9610482, 9612283, 9617277, 9710602, 3003594449, 3032109181
FEI numbers 3002808457, 3002808529, 3003190524, 3003309342, 3003513129, 3003594449, 3032109181
Establishment operations Manufacturer, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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