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 Life-Tech Instruments with 19 510(k) clearances. The most recent is a 510(k) clearance dated Sep 9, 1981: LIFE-TECH #1857 PRESSURE/POLOT MODULE.
| Date | Record | Source |
|---|---|---|
| Sep 9, 1981 | LIFE-TECH #1857 PRESSURE/POLOT MODULEK812177 · EXQ | 510(k) clearances |
| Aug 25, 1981 | LIFE-TECH #1753 BIOFEEDBACK TRAINERK812179 · HCC | 510(k) clearances |
| Aug 21, 1981 | LIFE-TECH #5102 VISULABK812180 · GWN | 510(k) clearances |
| Aug 13, 1981 | LIFE-TECH #'S 1106/1156 UROLABSK812178 · FAP | 510(k) clearances |
| Mar 10, 1980 | AMBLYOPIA TRAINERK800112 · HPL | 510(k) clearances |
| Apr 24, 1979 | MODEL 1750 STANDING URINALK790663 · FFG | 510(k) clearances |
| Apr 23, 1979 | MODEL 1309 AUDIO MONITORK790664 · IKN | 510(k) clearances |
| Nov 15, 1978 | MULAR GOLD LEAF ELECTRODE MODEL 7501K781476 · HLZ | 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
