# Healthtek, Inc.

- Location (FDA's records): Nevada City, CA
- FDA decisions: 9 (1985–1993): 9 510(k) clearances
- Product codes: LHI (4), KPE (2), GDM (1), FPB (1), FRN (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
- K923448: Empty Solution Transfer Container W/ Detach Leg (Jul 28, 1993)
- K913985: Transfer-Aid (TM) (Mar 18, 1992)
- K913608: Snapper (Nov 29, 1991)
- K881590: Adfuse (TM) (May 23, 1988)
- K874495: Adcomp 4000 HP System (Feb 16, 1988)
- K873848: Retrobulbar Needle (Oct 23, 1987)
- K860610: Adcomp (Jul 8, 1986)
- K860372: Fast Flow XX (Aqueous Solution Filter) (May 30, 1986)

Source page: https://510kreport.com/company/healthtek