FDA device listing
HCG Combo RapiDip™ InstaTest (Urine/Serum),OneStep HCG Combo RapiDip™ InstaTest (Urine/Serum)
FDA device listing 1153845763 · Diagnostic Automation /Cortez Diagnostics Inc.
Key facts
| Proprietary names | HCG Combo RapiDip™ InstaTest (Urine/Serum),OneStep HCG Combo RapiDip™ InstaTest (Urine/Serum) |
|---|---|
| Owner/operator | Diagnostic Automation /Cortez Diagnostics Inc. |
| Owner/operator number | 9011974 |
| Premarket submissions | K984080 |
| Product codes | JHI |
| Device names | JHI - Visual, Pregnancy Hcg, Prescription Use |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1155 |
| Review panels | Clinical Chemistry |
| Registered establishments | Diagnostic Automation/ Cortez Diagnostics Inc,. |
| Establishment registrations | 2029372 |
| FEI numbers | 1000306617 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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