The Ludlow Company LP
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K021132 | UNI-PATCH ULTRASOUND COUPLING GEL | MUI | 2002-05-15 | View |
| 510(k) | K012218 | LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODES | DRO | 2001-10-12 | View |
| 510(k) | K003511 | KENDALL-LTP TURNER SAVE-A-LINE | FRP | 2001-01-24 | View |
No matching devices.
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