MOTIONSPECT— 510(k) K895881

Name: FDA 510(k) clearance K895881
Creator: U.S. Food and Drug Administration
Published: 1990-04-10

Substantially Equivalent

Baltimore Therapeutic Equipment Co.

FDA 510(k) clearance K895881 for MOTIONSPECT, Substantially Equivalent on 1990-04-10. Applicant: Baltimore Therapeutic Equipment Co.. Device class: 3.

Clearance details

Applicant: Baltimore Therapeutic Equipment Co.
Product code: Code LXW
Device class: Class 3
Advisory panel: Unknown
Date received: 1989-10-05
Decision date: 1990-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hanover, MD, US

Download summary PDF View on FDA.gov ↗

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