Cardiac Pacemakers, Inc.
FDA 510(k) & PMA Approved Devices — 76 products
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Total Devices76
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K093969 | ACUITY BREAK-AWAY GUIDE CATHETER | DQY | 2010-03-05 | View |
| 510(k) | K080154 | ACUITY UNIVERSAL CUTTER | DQY | 2008-03-20 | View |
| 510(k) | K934727 | REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER | DWS | 1994-01-10 | View |
| 510(k) | K920601 | ASTRA T2, ASTRA T4, ASTRA T6 | DXY | 1992-10-28 | View |
| 510(k) | K912379 | PDT CARRYALL TRANSMITTER, VARIOUS MODELS | DXH | 1991-06-17 | View |
| 510(k) | K905674 | LEAD STYLET | DRB | 1991-01-30 | View |
| 510(k) | K900498 | MODIFIED BETATRON IV INSULIN INFUSION SYSTEM | LZG | 1990-02-23 | View |
| 510(k) | K894738 | MODEL 6888 LEAD TUNNELER | DWS | 1989-09-13 | View |
| 510(k) | K890785 | ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE | DXY | 1989-03-10 | View |
| 510(k) | K875147 | TORQUE HEX WRENCH | DTF | 1988-01-27 | View |
| 510(k) | K872774 | BETATRON IV SYSTEM | FRN | 1988-01-05 | View |
| 510(k) | K865013 | ASTRA T2, T4 AND T6 | DXY | 1987-02-19 | View |
| 510(k) | K863046 | ULTRA SOFTWARE MODULE: MODEL 2016 | KRG | 1986-12-05 | View |
| 510(k) | K863045 | PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580 | KRG | 1986-09-29 | View |
| 510(k) | K863000 | ASTRA 2,3,4 AND 6: CHIP REVISION | 1986-08-19 | View | |
| 510(k) | K860585 | ASTRA T2, T3, T4 & T6 MULTIPROGRAM PULSE GENERATOR | DXY | 1986-07-16 | View |
| 510(k) | K860584 | SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN | KRG | 1986-06-06 | View |
| 510(k) | K855171 | TELEMETRY WAND MODEL | DXY | 1986-01-22 | View |
| 510(k) | K852060 | INFUSION SETS MODELS 9120,9121,9125, 9122 & 9123 | FRN | 1985-06-07 | View |
| 510(k) | K842394 | ASTRA 2, ASTRA 3, 4 & 6 | DXY | 1984-10-17 | View |
No matching devices.
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