FDA 510(k) Applications Submitted by THE LUDLOW COMPANY LP

FDA 510(k) Number Submission Date Device Name Applicant
K012218 07/16/2001 LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODES THE LUDLOW COMPANY LP
K021132 04/09/2002 UNI-PATCH ULTRASOUND COUPLING GEL THE LUDLOW COMPANY LP


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact