LMA North America Inc
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assi recall (Z-2022-2012) | LMA North America Inc | 2012-07-17 |
| LMA- Unique Laryngeal Mask Airway Size 4, Catalog No. 12140, Lot FH041202 Size 4, Catalog recall (Z-1053-03) | LMA North America Inc | 2003-07-29 |
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Every clearance here is in the API, with alerts when new ones post.