Home › Device types › LZF
Pump, Infusion, Analytical Sampling
FDA product code LZF · Class 2 · General Hospital
2
Registered devices
2
Adverse events
1
Recalls
7
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-05-24 | International Biomedical, Ltd. | International Biomedical has received reports of interference between the collection bag and the extension set connectors. Evaluation of the affected components |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
