ClearanceBrief
Company ยท US

Ludlow Technical Products

FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 1999. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRXElectrode, Electrocardiograph1
FMTWarmer, Infant Radiant1
GEIElectrosurgical, Cutting & Coagulation & Accessories1
KXOMonitor, Pressure, Intrauterine1
NAEDressing, Wound, Hydrogel Without Drug And/Or Biologic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 8, 1999K991235SOFTRANS TEMP INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS TEMP IUPC)
Ludlow Technical Products
KXO
Oct 21, 1997K973110LUDLOW TECHNICAL PRODUCTS, ELECTRODE, ELECTROSURGICAL, DISPOSABLE PEDIATRIC DISPERSIVE ELECTRODES; WITH AND WITHOUT CORD
Ludlow Technical Products
GEI
Aug 21, 1997K972646AD-HEAL HYDROGEL DRESSING, VARIOUS SIZES
Ludlow Technical Products
NAE
Feb 6, 1997K964401KENDALL-LTP DISPOSABLE TEMPERATURE PROBES (DTP1,DTP2,DTP3,DTP4)
Ludlow Technical Products
FMT
Oct 7, 1993K931903SURELOCK(TM) SNAPLESS MONITORING ELECTRODE
Ludlow Technical Products
DRX

Latest recalls

DateFirm and productCodeLinked 510(k)
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