Medical Device Manufacturer · US , Mchenry , IL

Dobre, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1977
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Dobre, Inc. Cardiovascular ✕

2 devices
1-2 of 2
Cleared Jun 07, 1993
PLEXUS PULSER I, PLEXUS PULSER II
K924891 · JOW
Cardiovascular · 252d
Cleared Mar 29, 1977
ELECTROCARDIOGRAPHIC ELECTRODES, DISP.
K770521 · DRX
Cardiovascular · 11d
Filters
Filter by Specialty
All2 Cardiovascular 2