Leonhard Lang Medizintechnik GmbH
4 FDA 510(k) clearances · Recalling firm
◉ Watch Leonhard Lang Medizintechnik GmbH
| Record | Firm | Date |
|---|---|---|
| Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: M recall (Z-3109-2017) | Leonhard Lang Medizintechnik GmbH | 2017-09-12 |
| Skintact Electrodes for Defibrillation, DF29N. Product Usage: Multifunction electrode for recall (Z-0004-2017) | Leonhard Lang Medizintechnik GmbH | 2016-10-14 |
| ECG Electrodes: 50007 Stablebase SBW55 50675 Stablebase SBW55-15 58051 Skintact W-60 50547 recall (Z-0292-2016) | Leonhard Lang Medizintechnik GmbH | 2015-11-18 |
| Skintact ECG Electrode FS-50, Catalog no. 58028 , & Stable Base ECG Electrode SBT-60, Cata recall (Z-1350-2015) | Leonhard Lang Medizintechnik GmbH | 2015-03-28 |
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Every clearance here is in the API, with alerts when new ones post.