FDA device listing
Activated Carbon Filter,Biopsy Pad,Cassette Sponge
FDA device listing 1210872603 · Labworks Australia Pty Ltd
Key facts
| Proprietary names | Activated Carbon Filter,Biopsy Pad,Cassette Sponge |
|---|---|
| Owner/operator | Labworks Australia Pty Ltd |
| Owner/operator number | 10037346 |
| Product codes | KET |
| Device names | KET - Filters, Cell Collection, Tissue Processing |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.3010 |
| Review panels | Pathology |
| Registered establishments | LABWORKS AUSTRALIA PTY LTD |
| Establishment registrations | 3003919052 |
| FEI numbers | 3003919052 |
| Establishment operations | Manufacturer, Specification Developer |
| 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