TRIO 300— 510(k) K990787

Substantially Equivalent

Ito Co., Ltd.

FDA 510(k) clearance K990787 for TRIO 300, Substantially Equivalent on 1999-10-20. Applicant: Ito Co., Ltd.. Device class: 2.

Clearance details

Applicant: Ito Co., Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1999-03-10
Decision date: 1999-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, 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.