ERCHONIA PL2000— 510(k) K012580

Substantially Equivalent

Tuco Innovations, Inc.

FDA 510(k) clearance K012580 for ERCHONIA PL2000, Substantially Equivalent on 2002-01-17. Applicant: Tuco Innovations, Inc.. Device class: 2.

Clearance details

Applicant: Tuco Innovations, Inc.
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2001-08-09
Decision date: 2002-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Littleton, CO, US

Download summary PDF View on FDA.gov ↗

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