# Futuremed Div. of Future Impex Corp.

- Location (FDA's records): Deerpark, NY
- FDA decisions: 17 (1985–1994): 17 510(k) clearances
- Product codes: BZG (4), GZJ (3), EWO (2), GYB (2), GXY (1), DPS (1), IPF (1), BZM (1), BTY (1), KGO (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
- K933511: Upgraded Spirometer ST-90 (Feb 10, 1994)
- K933220: Selector SL 01 (Nov 24, 1993)
- K933222: Audiometer DA 323 (Nov 1, 1993)
- K903017: Mega-Tens Dual Channel T.E.N.S. (Oct 26, 1990)
- K901308: Spiro Analyzer Model ST 250 (Jul 23, 1990)
- K884972: Transcoutaneous Electro-Neuro Stimulator (Jul 27, 1989)
- K871421: Model HL-100 Portable DC Elect. Therapeutic Unit (Jan 22, 1988)
- K873817: Spiro Analyzer ST-300 (Dec 2, 1987)

Source page: https://510kreport.com/company/futuremed-div-of-future-impex