The Ludlow Company LP is one of 25722 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Ludlow Company LP - FDA 510(k) Cleared Devices
Recent clearances: UNI-PATCH ULTRASOUND COUPLING GEL, LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODES, KENDALL-LTP TURNER SAVE-A-LINE
3
Total
3
Cleared
0
Denied
The Ludlow Company LP has 3 FDA 510(k) cleared medical devices. Based in Chicopee, US.
Historical record: 3 cleared submissions from 2001 to 2002.
Browse the FDA 510(k) cleared devices submitted by The Ludlow Company LP Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Ludlow Company LP
3 devices