FDA device listing
Pipette Tip
FDA device listing 1862336056 · POLYMEDCO, INC.
Key facts
| Proprietary names | Pipette Tip |
|---|---|
| Owner/operator | POLYMEDCO, INC. |
| Owner/operator number | 9001475 |
| Product codes | JRC |
| Device names | JRC - Micro Pipette |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC. |
| Establishment registrations | 2435505 |
| FEI numbers | 1000119795 |
| Establishment operations | Complaint File Establishment |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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