← Back to catalogue
Modification To:xceed Nitinol Self-Expanding Transhepatic Biliary Stent System …
FDA 510(k)Class II (US FDA 510(k))
510(k) K032929
Identifiers
- 510(k) Number
- K032929 FDA 510(k)
- FDA Product Code
- FGE FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 876.5010 FDA 510(k)
- Regulation Number
- 876.5010 FDA 510(k)
- Advisory Committee
- Gastroenterology, Urology FDA 510(k)
- FDA Decision
- SESU FDA 510(k)
Modification To:xceed Nitinol Self-Expanding Transhepatic Biliary Stent System … by Abbott Vascular Inc. — Class II — FDA_510K — listed in FDA 510(k) — 5 models
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 | K032929 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Abbott Vascular Inc.
- FDA Applicant
- Abbott Vascular, Inc.
Sources (1)
- FDA 510(k) K032929 24 fields · synced Jun 18, 2026