Edwards Pacemaker Systems
FDA 510(k) medical device clearances.
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.