Edwards Pacemaker Systems
Edwards Pacemaker Systems holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1979.
Top product codes for Edwards Pacemaker Systems
Recent clearances by Edwards Pacemaker Systems
- K791751 — EDWARDS PACEMAKER 30 UNIPOLAR GENERATOR
- K790452 — 28 UNIPOLAR AND BIPOLAR PULSE GENERATORS
- K781111 — LEAD CONVERSION KIT, MODEL 341
- K781144 — ANALYZER, PACER SYSTEM, PSA-5
- K781042 — PROLITH 23S PACEMAKER
- K780780 — MICROPULSE 22S PACEMAKER
- K780238 — PACEMAKER, PROLITH 23U. PULSE GENERATOR
- K780091 — MICROPULSE 22U
- K771987 — MICROPULSE 26U PULSE GENERATOR
- K770656 — GENERATOR, PULSE, CARDIAC 20U
- K770657 — GENERATOR, PULSE, CARDIAC 2LU
- K770212 — PROLITH MODEL 21S CARDIAC PULSE GEN.
- K770211 — MICROPULSE MODEL 20S
Data sourced from openFDA. This site is unofficial and independent of the FDA.