# Baltimore Therapeutic Equipment Co.

- Location (FDA's records): Hanover, MD
- FDA decisions: 7 (1980–1995): 7 510(k) clearances
- Product codes: BXB (3), KQX (1), LXW (1), IKK (1), ISD (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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K955105: Bte CPM-10 (Dec 29, 1995)
- K955106: Bte CPM-20 (Dec 29, 1995)
- K925225: The Bte Vector; Analysis System for the Low Back (Jun 27, 1994)
- K933611: The Bte WS30 (Jun 20, 1994)
- K924414: The Bte Dynamic Lift (Feb 12, 1993)
- K895881: Motionspect (Apr 10, 1990)
- K800007: Work Simulator (Jan 21, 1980)

Source page: https://510kreport.com/company/baltimore-therapeutic-equipment