Analyzer, Pacemaker Generator Function, Indirect
FDA product code KRE · 13 cleared devices
Class 2
Cardiovascular
- Regulation
- 21 CFR 870.3640
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1980-05-28 – 2011-06-08
KRE
2011-06-08
KRE
2008-08-22
CYGNUS 12 LEAD ECG MODULE
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KRE
2003-10-15
EKG SPEAKS
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KRE
1993-03-18
HPM 40 HEART PACEMAKER MONITOR
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KRE
1992-04-14
PACEART CPTS-86/12
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KRE
1990-03-19
PACEVIEW
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KRE
1987-04-27
PACEMAKER FUNCTION ANALYZER
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KRE
1983-12-16
PACEMAKER SYS ANALYZER #384
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KRE
1983-11-14
PACEMAKER SYS. ANALYZER 378
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KRE
1981-03-17
CARDIOMEMO
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KRE
1980-08-14
ELECTRONIC PACEMAKER WAVEFORM ANALYZER
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KRE
1980-06-17
ULTRA-CHEK PACEMAKER MONITOR
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KRE
1980-05-28
PACE-PULSE/COMPUTRAC
View details →No matching devices.
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