MOBILIMB H3 HAND CPM UNIT— 510(k) K900794

Name: FDA 510(k) clearance K900794
Creator: U.S. Food and Drug Administration
Published: 1990-03-02

Substantially Equivalent

Toronto Medical Corp.

FDA 510(k) clearance K900794 for MOBILIMB H3 HAND CPM UNIT, Substantially Equivalent on 1990-03-02. 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: 1990-02-20
Decision date: 1990-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada L1w2y5, CA

Download summary PDF View on FDA.gov ↗

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K921351 — JACE MODEL PM-410 HAND CPM DEVICE1992-05-04
K900581 — DANNIFLEX CPM 880(TM)1990-02-20

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K925926 — MOBILIMB T1 TOE CPM UNIT1993-03-22
K900466 — MOBILIMB W1 WRIST CPM UNIT1990-03-12

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