ULTRA III— 510(k) K960096

Name: FDA 510(k) clearance K960096
Creator: U.S. Food and Drug Administration
Published: 1996-03-27

Substantially Equivalent for Some Indications

Excel Tech. , Ltd.

FDA 510(k) clearance K960096 for ULTRA III, Substantially Equivalent for Some Indications on 1996-03-27. Applicant: Excel Tech. , Ltd.. Device class: 2.

Clearance details

Applicant: Excel Tech. , Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1996-01-11
Decision date: 1996-03-27
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Oakville,Ontario, CA

Download summary PDF View on FDA.gov ↗

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