# Medprobe Laboratories

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1982–1983): 4 510(k) clearances
- Product codes: FMK (4)
- 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
- K833816: Hemastick 1-1.5 & 2-Dispos. Blood (Dec 22, 1983)
- K830001: Superjet BTD Bleeding Time Device Disp (Sep 26, 1983)
- K830010: Superjet Lancet (Jan 26, 1983)
- K820625: Hemalet Automatic Lancet Device (Apr 9, 1982)

Source page: https://510kreport.com/company/medprobe-laboratories