Cardiac Pacemakers, Inc.
Cardiac Pacemakers, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2010.
Top product codes for Cardiac Pacemakers, Inc.
Recent clearances by Cardiac Pacemakers, Inc.
- K093969 — ACUITY BREAK-AWAY GUIDE CATHETER
- K080154 — ACUITY UNIVERSAL CUTTER
- K934727 — REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER
- K920601 — ASTRA T2, ASTRA T4, ASTRA T6
- K912379 — PDT CARRYALL TRANSMITTER, VARIOUS MODELS
- K905674 — LEAD STYLET
- K900498 — MODIFIED BETATRON IV INSULIN INFUSION SYSTEM
- K894738 — MODEL 6888 LEAD TUNNELER
- K890785 — ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE
- K875147 — TORQUE HEX WRENCH
- K872774 — BETATRON IV SYSTEM
- K865013 — ASTRA T2, T4 AND T6
- K863046 — ULTRA SOFTWARE MODULE: MODEL 2016
- K863045 — PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580
- K863000 — ASTRA 2,3,4 AND 6: CHIP REVISION
- K860585 — ASTRA T2, T3, T4 & T6 MULTIPROGRAM PULSE GENERATOR
- K860584 — SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN
- K855171 — TELEMETRY WAND MODEL
- K852060 — INFUSION SETS MODELS 9120,9121,9125, 9122 & 9123
- K842394 — ASTRA 2, ASTRA 3, 4 & 6
- K842364 — HANDHELD PACEMAKER PROGRAMMER & SOFTWAR
- K843060 — SENTRA
- K833306 — BETATRON I AMBULATORY INSULIN PUMP
- K831216 — COMMAND ULTRA II
- K831161 — COMMAND ULTRA I
- K831160 — LEAD ADAPTERS #'S 6016,6022,6017 ETC
- K831259 — RESERVOIR 1.5CC #9210 W/25 GAUGE/NEEDLE
- K830382 — COMMAND ULTRA II
- K822857 — CPI PRINTER
- K823204 — BETATRON II
- K822774 — 9110 SYRINGE
- K822775 — INFUS. SETS-9120-50 CM & 9121-100 CM,EXT
- K822776 — TEFLON CANNULA
- K822309 — COMMAND NP
- K820230 — PACEMAKER PROGRAMMER 2030
- K820231 — COMMAND ULTRA I
- K820073 — OPEN LOOP AMBULATORY INSULIN INFUSION
- K813534 — COMMAND P5
- K812917 — PORTABLE LIDOCAINE INFUSION PUMP
- K811401 — COMMAND P5(UNIPOLAR PULSE GENERATOR)
- K811402 — COMMAND P5(BIPOLAR PULSE GENERATOR)
- K811217 — PACEMAKER PROGRAMMER #2010
- K811774 — OPEN LOOP AMBULATORY INFUSION DEVICE
- K802352 — MICRO THIN-DII, #0521
- K802353 — MICRO THIN-PII, #0523
- K803034 — MICROTHIN-PII BIPOLAR PULSE GEN. #0623
- K803035 — MICROTHIN-PII BIPOLAR PULSE GEN. #0621
- K802058 — MAPPING PROBE MODEL #6540
- K802409 — MICROTHIN-DI BIPOLAR PULSE GENERATOR
- K802410 — MICROTHIN-PI BIPOLAR PULSE GENERATOR
- K802077 — UNIPOLAR TO BIPOLAR PULSE GEN. ADAPTER
- K802076 — STIFF STYLETS
- K802089 — CARDIOTRAK
- K801121 — MICROTHIN-P1 (MOD. 0622)
- K801122 — MICROTHIN-D1 (MOD. 0620)
- K800026 — MICROTHIN-DI
- K800027 — MICROTHIN-PI
- K792580 — PACEMAKER PROGRAMMER
- K790503 — CARDIOTEST 2200
- K790432 — MICROLITH MODELS 505; 605; 507; 607; 703; 803
- K790276 — MINILITH AND MICROLITH
- K782022 — MICROLITH A MODEL 703
- K782023 — MICROLITH A MODEL 803
- K772238 — PULSE GENERATOR, UNIPOLAR, PROGRAMABLE
- K772239 — PULSE GENERATOR, BIPOLAR, PROGRAMMABLE
- K772240 — PULSE GENERATOR, UNIPOLAR, DEMAND
- K772241 — PULSE GENERATOR, BIPOLAR, DEMAND
- K770880 — GENERATOR, PULSE, UNIPOLAR, #508
- K770881 — GENERATOR, PULSE, BIPOLAR 3608
- K770716 — GENERATOR, PULSE, UNIPOLAR, MODEL #504
- K770715 — GENERATOR, PULSE, BIPOLAR, MODEL #604
- K770243 — ELGILOY STYLET
- K770197 — UNIPOLAR, ASYNCHRONOUS PULSE GENERATOR
- K770198 — BIPOLAR ASYNCHRONOUS PULSE GENERATOR
- K770199 — LEAD EXTENDER MODEL 6516
- K770042 — ADAPTER, LEAD, GENERAL ELECTRIC
Data sourced from openFDA. This site is unofficial and independent of the FDA.