Ludlow Technical Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ludlow Technical Products - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Ludlow Technical Products has 5 FDA 510(k) cleared medical devices. Based in Chicopee, US.
Historical record: 5 cleared submissions from 1993 to 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ludlow Technical Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ludlow Technical Products
5 devices
Cleared
Jul 08, 1999
SOFTRANS TEMP INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS TEMP...
Obstetrics & Gynecology
87d
Cleared
Oct 21, 1997
LUDLOW TECHNICAL PRODUCTS, ELECTRODE, ELECTROSURGICAL, DISPOSABLE PEDIATRIC...
General & Plastic Surgery
62d
Cleared
Aug 21, 1997
AD-HEAL HYDROGEL DRESSING, VARIOUS SIZES
General & Plastic Surgery
37d
Cleared
Feb 06, 1997
KENDALL-LTP DISPOSABLE TEMPERATURE PROBES (DTP1,DTP2,DTP3,DTP4)
General Hospital
94d
Cleared
Oct 07, 1993
SURELOCK(TM) SNAPLESS MONITORING ELECTRODE
Cardiovascular
175d