FDA Device Establishments · JSON-LD · Markdown
FEI 3010334444 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3010334444 |
|---|---|
| Owner / Operator | Ablative Solutions, Inc. (#10044459) |
| Address | 301 Edgewater Place, Suite 100, Wakefield, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KRA |
| Regulation § (21 CFR) | 870.1210 |
| Proprietary names | Peregrine System(TM) Infusion Catheter |
Source: openFDA. Public-domain (CC0).