Ludlow Technical Products

FDA Regulatory Profile

Ludlow Technical Products appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 8, 1999.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K991235SOFTRANS TEMP INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS TEMP IUPC)July 8, 1999
K973110LUDLOW TECHNICAL PRODUCTS, ELECTRODE, ELECTROSURGICAL, DISPOSABLE PEDIATRIC DISPERSIVE ELECTRODES; WOctober 21, 1997
K972646AD-HEAL HYDROGEL DRESSING, VARIOUS SIZESAugust 21, 1997
K964401KENDALL-LTP DISPOSABLE TEMPERATURE PROBES (DTP1,DTP2,DTP3,DTP4)February 6, 1997
K931903SURELOCK(TM) SNAPLESS MONITORING ELECTRODEOctober 7, 1993