Data / Medical devices / United States / Cambridge Interventional LLC
Cambridge Interventional LLC: FDA-registered device maker in Burlington, MA, United States, 1 510(k) clearance
Cambridge Interventional LLC is registered with the FDA (registration 3015257340) in Burlington, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 7, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015257340
- Address
- 78 Cambridge St., Burlington, MA, United States, 01803
- Owner or operator
- Cambridge Interventional LLC (10062374)
- Roles
- Manufacturer
- First device listed
- January 17, 2020
- Registered through
- 2026
- Brand names listed
- CRF Radiofrequency Ablation System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| January 7, 2020 | K192715 | CRF Radiofrequency Ablation System | GEI | Substantially Equivalent | Cambridge Interventional, LLC | accessdata.fda.gov |
Compare with other makers
Updated January 7, 2020. 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.