Arco Medical Products Co.
Arco Medical Products Co. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1980.
Top product codes for Arco Medical Products Co.
Recent clearances by Arco Medical Products Co.
- K802588 — MODEL 3003 UNIPOLAR DEMAND CARDIAC GEN.
- K801806 — EXTERNAL SILASTIC BOOT FOR CARDIAC PULSE
- K800837 — PROGRAMMABLE BIPOLAR CARDIAC GENERATOR
- K801241 — UNIPOLAR PROGRAMMABLE LITHIUM CARD. GEN.
- K800838 — ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN.
- K800326 — ARCOLITH 3021-CARDIAC PULSE GENERATOR
- K792216 — ARCOLITH 2100-CARDIAC PULSE GENERATOR
- K792299 — ARCOLITH 3020-CARDIAC PULSE GENERATOR
- K791715 — ARCOLITH 2000
- K791147 — ARCO PROGAMMABLE PACEMAKER SYSTEM
- K791165 — ARCOLITH 4000
- K790436 — IMPLANTABLE HEART LEAD TERMINAL ADAPTER
- K790468 — IMPLANTABLE HEART LEAD EXTENDER
- K782146 — PACEMAKER, MODEL DDP ELECTRONIC CIRCUIT
- K780776 — ARCOBIOLITH PACEMAKER MODEL
- K780297 — CARDIAC MINISCOPE & MINIGRAPH
- K780307 — CARDIAC MINIGRAPH
- K771262 — PACEMAKER & CARDIAC LEAD, BIPOLAR
- K770416 — LEAD, HEART, BUTTERFLY CLAMP
- K761237 — ELEC. CIR. PACE. MO. LI-2,LI-3,LI-4,LI-5
- K760963 — DECUBITUS MATTRESS
Data sourced from openFDA. This site is unofficial and independent of the FDA.