FDA applicant
Baltimore Therapeutic Equipment Co.
FDA records 7 decisions for Baltimore Therapeutic Equipment Co. (Hanover, MD) from 1980 to 1995: 7 510(k) clearances. Most are in product codes BXB (Exerciser, Powered) and KQX (Goniometer, Ac-Powered). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Baltimore Therapeutic Equipment Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Baltimore Therapeutic Equipment Co. since 2007.
Recalls per year
1in 2015
Class I Class II/III not classified
Planning a device like Baltimore Therapeutic Equipment Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report