Medical Device Manufacturer · US , Salem , NH

Memtec Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997

Recent clearances: MOBILEECG SYSTEM, MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSIS, MODEL 700

View 3 510(k) Devices ↓
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Memtec Corp. Cardiovascular ✕

3 devices
1-3 of 3
Cleared Mar 24, 2011
MOBILEECG SYSTEM
K103427 · DPS
Cardiovascular · 122d
Cleared Dec 09, 2010
MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSIS
K102723 · MWJ
Cardiovascular · 79d
Cleared Mar 07, 1997
MODEL 700
K944180 · DSH
Cardiovascular · 924d
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