# Pharmaquest Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1981–1995): 14 510(k) clearances
- Product codes: FOH (4), GYE (3), BTY (2), CGA (2), MPG (1), FMA (1), CBK (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
- K945519: Face (Fluorophore-Assisted-Carbohydrate-Electrophoresis) Urinary Carbohydrate Analysis System (Nov 3, 1995)
- K833236: Telephone Transmitter T-10 Eeg (Nov 29, 1983)
- K833880: Telephonic Receiver R-10 Eeg (Nov 29, 1983)
- K830705: Mini Lancet-Blood Lancet (Apr 8, 1983)
- K822976: Hypocount a (Nov 16, 1982)
- K822486: Home Blood Glucose Monitor (Nov 5, 1982)
- K820248: Rodder Volume Ventilator (Apr 16, 1982)
- K812850: PTT-200 Pulmonary Receiver/Microproces (Dec 3, 1981)

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