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/ The Ludlow Company LP
The Ludlow Company LP
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K021132
UNI-PATCH ULTRASOUND COUPLING GEL
May 15, 2002
K012218
LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODES
October 12, 2001
K003511
KENDALL-LTP TURNER SAVE-A-LINE
January 24, 2001