Data / Medical devices / United States / Liquet Medical Inc.
Liquet Medical Inc.: FDA-registered device maker in Glen Allen, VA, United States, 1 510(k) clearance
Liquet Medical Inc. is registered with the FDA (registration 3038791046) in Glen Allen, VA, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 25, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3038791046
- Address
- 5619 Country Hills Ln, Glen Allen, VA, United States, 23059
- Owner or operator
- Liquet Medical Inc. (10093653)
- Roles
- Specification developer
- First device listed
- June 17, 2025
- Registered through
- 2026
- Brand names listed
- Versus Catheter VS110-8B
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Continuous Flush | KRA | 2 | Specification developer | accessdata.fda.gov |
| Catheter, Flow Directed | DYG | 2 | Specification developer | accessdata.fda.gov |
| Catheter, Intravascular, Diagnostic | DQO | 2 | Specification developer | accessdata.fda.gov |
| Mechanical Thrombolysis Catheter | QEY | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 25, 2024 | K241851 | Versus Catheter (VS110-8B) | QEY | Substantially Equivalent | Liquet Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Continuous Flush
- All makers of Catheter, Intravascular, Diagnostic
- All makers of Catheter, Flow Directed
- All makers of Mechanical Thrombolysis Catheter
Updated November 25, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.