FDA.reportPublic FDA data

Device Listing 1191292518

Listing Summary#

Listing key
1191292518
Premarket submission
K101660
Device
ECG SINGLE PATIENT USE LEAD WIRE SET, MODELS 2048801-5 TO 2048801-8
Applicant
Kepler Medtec
Product code
DSA
Decision date
2010-08-11