MOTIONSPECT— 510(k) K895881

Substantially Equivalent

Baltimore 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
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.