ALIMAXX-B UNCOVERED BILIARY STENT SYSTEM— 510(k) K072720
UnknownAlveolus, Inc.
FDA 510(k) clearance K072720 for ALIMAXX-B UNCOVERED BILIARY STENT SYSTEM, Unknown on 2008-04-11. Applicant: Alveolus, Inc.. Device class: 2.
Clearance details
- Applicant
- Alveolus, Inc.
- Product code
- Code FGE
- Device class
- Class 2
- Regulation
- 21 CFR 876.5010
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Charlotte, NC, US
Recent devices under product code FGE
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- K253832 — Dilation Balloon Catheter
- K251658 — Endoflux Biliary & Pancreatic Stent Sets
- K253987 — BARE Wireguided Balloon Dilation Catheter (1235)
More clearances from Alveolus, Inc.
view allAdverse events under product code FGE
product code FGE- Death
- 52
- Injury
- 2,347
- Malfunction
- 9,798
- Other
- 1
- Total
- 12,198
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.