Medical Device Manufacturer · US , Ashland , MA

Kepler Medtec - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Kepler Medtec Cardiovascular ✕

1 devices
1-1 of 1
Cleared Aug 11, 2010
ECG SINGLE PATIENT USE LEAD WIRE SET, MODELS 2048801-5 TO 2048801-8
K101660 · DSA
Cardiovascular · 58d
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All2 General & Plastic Surgery 1 Cardiovascular 1