FDA device listing
ADVANCED DIGITAL ULTRASOUND SYSTEM (HV-PREIRUS),HITACHI ARIETTA 70 ULTRASOUND SCANNER (EUS-ARIETTA 70),LINEAR ULTRASOUND…
FDA device listing 1576165984 · HOYA Corporation PENTAX Division
Key facts
| Proprietary names | ADVANCED DIGITAL ULTRASOUND SYSTEM (HV-PREIRUS),HITACHI ARIETTA 70 ULTRASOUND SCANNER (EUS-ARIETTA 70),LINEAR ULTRASOUND VIDEO GASTROSCOPE (EG-3870UTK),OPTIVISTA HD VIDEO PROCESSOR(EPK-I7010),ULTRASOUND VIDEO GASTROSCOPE (EG-3270UK),ULTRASOUND VIDEO GASTROSCOPE (EG-3670URK),VIDEO PROCESSOR (EPK-i5010) |
|---|---|
| Owner/operator | HOYA Corporation PENTAX Division |
| Owner/operator number | 8030235 |
| Premarket submissions | K182004 |
| Product codes | ITX, ODG |
| Device names | ITX - Transducer, Ultrasonic, Diagnostic, ODG - Endoscopic Ultrasound System, Gastroenterology-Urology |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500, 892.1570 |
| Review panels | Gastroenterology & Urology, Radiology |
| Registered establishments | HOYA Corporation PENTAX Lifecare Division, PENTAX MEDICAL (PENANG) SDN. BHD. |
| Establishment registrations | 9610877, 3003782610, 3014605202 |
| FEI numbers | 3003782610, 3008185830, 3014605202 |
| Establishment operations | Complaint File Establishment, Specification Developer, Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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