Bunnell, Inc.
5 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort End recall (Z-0371-2023) | Bunnell, Inc. | 2022-12-03 |
| Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is recall (Z-0514-2013) | Bunnell, Inc. | 2012-12-14 |
| One Cat. Life Pulse High Frequency Ventilator, Catalog Number: 203A, Manufactured by: Bunn recall (Z-0901-2011) | Bunnell, Inc. | 2011-01-14 |
| One Cat. Life Pulse High Frequency Ventilator, Catalog Number: 203, Manufactured by: Bunne recall (Z-0902-2011) | Bunnell, Inc. | 2011-01-14 |
| Life Pulse High Frequency Ventilator (HFV) recall (Z-0893-06) | Bunnell, Inc. | 2006-05-23 |
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Every clearance here is in the API, with alerts when new ones post.