# Medtel Pty., Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1979–1983): 8 510(k) clearances
- Product codes: DRT (4), DSK (2), FLL (1), BZN (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
- K832356: Portable Operat. RM. Monitors HS30/40 (Oct 28, 1983)
- K820670: HS17/HS18 Series Monitors (Apr 9, 1982)
- K820671: CM10 Central Monitoring System (Apr 1, 1982)
- K820399: HS20 Port. Operating Room Monitor (Mar 22, 1982)
- K802184: HS10 Portable Operating Room Monitor (Sep 26, 1980)
- K800243: D668 & D664 Central Monitoring Systems (Apr 10, 1980)
- K791839: H59 Critical Care Monitor (Oct 1, 1979)
- K791838: HSH/H512 Adult Physiological Monitors (Oct 1, 1979)

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