MOBILIMB CPM SHOULDER UNIT— 510(k) K891345

Name: FDA 510(k) clearance K891345
Creator: U.S. Food and Drug Administration
Published: 1989-04-24

Substantially Equivalent

Toronto Medical Corp.

FDA 510(k) clearance K891345 for MOBILIMB CPM SHOULDER UNIT, Substantially Equivalent on 1989-04-24. Applicant: Toronto Medical Corp.. Device class: 1.

Clearance details

Applicant: Toronto Medical Corp.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1989-03-09
Decision date: 1989-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, D.C., DC, US

Download summary PDF View on FDA.gov ↗

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