MULTI III— 510(k) K921953

Substantially Equivalent

Excel Tech. , Ltd.

FDA 510(k) clearance K921953 for MULTI III, Substantially Equivalent on 1992-08-26. Applicant: Excel Tech. , Ltd.. Device class: 2.

Clearance details

Applicant
Excel Tech. , Ltd.
Product code
Code LIH
Device class
Class 2
Regulation
21 CFR 882.5890
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Oakville,Ontario, CA
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Data sourced from openFDA. This site is unofficial and independent of the FDA.