MOTIONSPECT— 510(k) K895881
Substantially EquivalentBaltimore Therapeutic Equipment Co.
FDA 510(k) clearance K895881 for MOTIONSPECT, Substantially Equivalent on 1990-04-10. Applicant: Baltimore Therapeutic Equipment Co..
Clearance details
- Applicant
- Baltimore Therapeutic Equipment Co.
- Product code
- Code LXW
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hanover, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.