MOBILIMB HAND C.P.M. UNIT— 510(k) K880336

Name: FDA 510(k) clearance K880336
Creator: U.S. Food and Drug Administration
Published: 1988-02-16

Substantially Equivalent

Toronto Medical Corp.

FDA 510(k) clearance K880336 for MOBILIMB HAND C.P.M. UNIT, Substantially Equivalent on 1988-02-16. Applicant: Toronto Medical Corp.. Device class: 1.

Clearance details

Applicant: Toronto Medical Corp.
Product code: Code JFA
Device class: Class 1
Regulation: 21 CFR 890.5410
Advisory panel: Physical Medicine
Date received: 1988-01-26
Decision date: 1988-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yellow Springs, OH, 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.