Medcor, Inc.
Medcor, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1980.
Top product codes for Medcor, Inc.
Recent clearances by Medcor, Inc.
- K792609 — LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN.
- K802223 — QUINTREX 0515 PROGRAMMABLE PULSE GEN.
- K802224 — QUINTREX 0516 PROG. PULSE GENERATOR SYS
- K791678 — LITHICRON II 0403 IMPLANTABLE PACEMAKER
- K791095 — LITHICRON MODEL 0401, PACEMAKER
- K780430 — LITHICRON F PROGRAMMABLE PULSE GEN
- K771538 — LITHICRON MODEL 3-70C-B PULSE GENERATOR
- K770507 — PULSE GENERATOR, LITKICRON MODEL 3-70H
Data sourced from openFDA. This site is unofficial and independent of the FDA.