FDA device listing
SteriScan Reusable Test Pack (5500) (FP-CFE),VERIFY All-In-One STEAM Reusable Test Pack (LCB039) (FP-CFE),VERIFY…
FDA device listing 1735289032 · STERIS Corporation
Key facts
| Proprietary names | SteriScan Reusable Test Pack (5500) (FP-CFE),VERIFY All-In-One STEAM Reusable Test Pack (LCB039) (FP-CFE),VERIFY All-In-One STEAM Reusable Test Pack (LCB055) (FP-MF, HP-MF),VERIFY All-In-One STEAM Reusable Test Pack with Step Counter (LCB040) (FP-CFE),VERIFY All-In-One STEAM Reusable Test Pack with Tag (LCB041) (FP-CFE) |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10078069 |
| Premarket submissions | K102761 |
| Product codes | JOJ |
| Device names | JOJ - Indicator, Physical/Chemical Sterilization Process |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.2800 |
| Review panels | General Hospital |
| Registered establishments | STERIS Corporation |
| Establishment registrations | 3000251274, 3007412809 |
| FEI numbers | 3000251274, 3007412809 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| 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