Belmont Instrument LLC
6 FDA 510(k) clearances · Recalling firm
◉ Watch Belmont Instrument LLC
| Record | Firm | Date |
|---|---|---|
| Allon 2001. Part Number: 200-00263 recall (Z-1966-2025) | Belmont Instrument LLC | 2025-06-12 |
| Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile, single-use, disposable recall (Z-1674-2025) | Belmont Instrument LLC | 2025-04-25 |
| Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile, single-use, di recall (Z-1675-2025) | Belmont Instrument LLC | 2025-04-25 |
| Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038. Sterile, single-use, recall (Z-1676-2025) | Belmont Instrument LLC | 2025-04-25 |
| 3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The P/N 903-00032 consist recall (Z-1678-2025) | Belmont Instrument LLC | 2025-04-25 |
| Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser RI-2. Designed recall (Z-1099-2025) | Belmont Instrument LLC | 2025-02-04 |
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Every clearance here is in the API, with alerts when new ones post.