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The Ludlow Company LP

FDA Regulatory Profile

The Ludlow Company LP appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 15, 2002.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K021132UNI-PATCH ULTRASOUND COUPLING GELMay 15, 2002
K012218LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODESOctober 12, 2001
K003511KENDALL-LTP TURNER SAVE-A-LINEJanuary 24, 2001

FDA data resources