Programmer, Pacemaker
FDA product code KRG · 25 cleared devices
Class 3
Cardiovascular
- Regulation
- 21 CFR 870.3700
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1977-10-07 – 1995-03-15
KRG
1995-03-15
KRG
1989-08-25
MODEL 5650 OPTIMATE PERSONAL PROGRAMMER
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KRG
1988-11-17
MODEL 2331T PATIENT PROGRAMMER
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KRG
1988-07-22
MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004
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KRG
1987-12-17
MODEL 1740 PERSONAL POCKET PROGRAMMER
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KRG
1987-06-24
MODEL 5600B PROGRAMMER, PACEMAKER
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KRG
1986-12-05
ULTRA SOFTWARE MODULE: MODEL 2016
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KRG
1986-09-29
PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580
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KRG
1986-06-06
SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN
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KRG
1986-04-23
DIALOG PROGRAMMER 700 - PROGRAM VERSION 6.37
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KRG
1985-07-24
HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA
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KRG
1985-04-19
CERYX6, 611, CERYX 3 311 & CERYX 1 111
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KRG
1985-04-19
TP 1
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KRG
1984-09-24
HANDHELD PACEMAKER PROGRAMMER & SOFTWAR
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KRG
1982-03-15
PACEMAKER PROGRAMMER 2030
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KRG
1981-11-02
FLOW-DIRECTED BALLOON THERMODILUTION
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KRG
1981-10-27
INTERMEDICS PROGRAMMER, MODEL 522-03
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KRG
1981-07-20
PACEMAKER PROGRAMMER #2010
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KRG
1981-03-20
CORDIS PACEMAKER PROGRAMMERS 255A & 256A
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KRG
1980-04-21
EPR-200 PROGRAMMER MODEL 010
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KRG
1979-12-19
PACEMAKER PROGRAMMER
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KRG
1979-11-27
OMNICOR PROGRAMMER MODEL 222C
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KRG
1979-07-31
PACEMAKER PROGRAMMER
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KRG
1978-04-21
RATE PROGRAMMER MODEL 520
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KRG
1977-10-07
OMNICOR PROGRAMMER MODEL 222A
View details →No matching devices.
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