Leonhard Lang Gmbh
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing Electrodes. REF 2059 recall (Z-0802-2015) | Leonhard Lang Gmbh | 2014-12-19 |
| SKINTACT Electrodes for Defibrillation, 10X REF DF20, Rx only, Manufactured by Leonhard La recall (Z-2233-2009) | Leonhard Lang Gmbh | 2009-09-24 |
| S&W Electrodes for Defibrillation, 10 Defibrillation Electrodes, Reorder #90101, S & W Hea recall (Z-2234-2009) | Leonhard Lang Gmbh | 2009-09-24 |
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