← Back to catalogue
EchoTip AcuCore™ EUS Biopsy Needle (ECHO-BX-19)
FDA 510(k)Class II (US FDA 510(k))
510(k) K241209
Identifiers
- 510(k) Number
- K241209 FDA 510(k)
- FDA Product Code
- FCG FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 876.1075 FDA 510(k)
- Regulation Number
- 876.1075 FDA 510(k)
- Advisory Committee
- Gastroenterology, Urology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
EchoTip AcuCore™ EUS Biopsy Needle (ECHO-BX-19) by Cook Ireland, Ltd. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K241209 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cook Ireland, Ltd.
Sources (1)
- FDA 510(k) K241209 24 fields · synced Jun 18, 2026