Leonhard Lang Co.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K024264 | SKINTACT | DRX | 2003-01-16 | View |
| 510(k) | K982521 | SKINTACT ECG ELECTRODES, S&W ECG ELECTRODES | DRX | 1999-10-26 | View |
No matching devices.
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