Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Lumiscope Co., Inc. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Oct 22, 2003: CARDICARE MODEL MT-301F & MT-301C.
| Oct 22, 2003 | CARDICARE MODEL MT-301F & MT-301CK032714 · FLL | 510(k) clearances |
| Jun 21, 1996 | LUMISCOPE MODEL 2018 THERMOMETERK954792 · FLL | 510(k) clearances |
| Feb 23, 1994 | INTERFERENTIAL CURRENT THERAPY UNITK931768 · LIH | 510(k) clearances |
| Jun 29, 1993 | INFRARED LAMPK925054 · ILY | 510(k) clearances |
| Nov 9, 1992 | LUMISONICK924081 · CAF | 510(k) clearances |
| Mar 9, 1992 | GYMMANK920099 · DRT | 510(k) clearances |
| Aug 24, 1990 | LUMISCOPE EMS 8000K901849 · IPF | 510(k) clearances |
| Aug 21, 1990 | LUMISCOPE ALTERNATING PRESSURE PAD & PUMPK901096 · FNM | 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
