# Life-Tech Instruments, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 19 (1977–1981): 19 510(k) clearances
- Product codes: IKN (2), GWJ (2), FAP (2), GWF (1), FFG (1), HPL (1), HLZ (1), EWO (1), EXY (1), GXY (1), HCC (1), GWK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K812177: Life-Tech #1857 Pressure/Polot Module (Sep 9, 1981)
- K812179: Life-Tech #1753 Biofeedback Trainer (Aug 25, 1981)
- K812180: Life-Tech #5102 Visulab (Aug 21, 1981)
- K812178: Life-Tech #'S 1106/1156 Urolabs (Aug 13, 1981)
- K800112: Amblyopia Trainer (Mar 10, 1980)
- K790663: Model 1750 Standing Urinal (Apr 24, 1979)
- K790664: Model 1309 Audio Monitor (Apr 23, 1979)
- K781476: Mular Gold Leaf Electrode Model 7501 (Nov 15, 1978)

Source page: https://510kreport.com/company/life-tech-instruments