Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Medcor, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Nov 19, 1980: LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN..
| Date | Record | Source |
|---|---|---|
| Nov 19, 1980 | LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN.K792609 · DXY | 510(k) clearances |
| Sep 12, 1980 | QUINTREX 0515 PROGRAMMABLE PULSE GEN.K802223 · | 510(k) clearances |
| Sep 12, 1980 | QUINTREX 0516 PROG. PULSE GENERATOR SYSK802224 · | 510(k) clearances |
| Sep 7, 1979 | LITHICRON II 0403 IMPLANTABLE PACEMAKERK791678 · DXY | 510(k) clearances |
| Aug 10, 1979 | LITHICRON MODEL 0401, PACEMAKERK791095 · DXY | 510(k) clearances |
| Dec 22, 1978 | LITHICRON F PROGRAMMABLE PULSE GENK780430 · DXY | 510(k) clearances |
| Aug 22, 1977 | LITHICRON MODEL 3-70C-B PULSE GENERATORK771538 · DXY | 510(k) clearances |
| Apr 7, 1977 | PULSE GENERATOR, LITKICRON MODEL 3-70HK770507 · DXY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
