THE LEADAWAY— 510(k) K992372

Substantially Equivalent

Therapy Equipment, Inc.

FDA 510(k) clearance K992372 for THE LEADAWAY, Substantially Equivalent on 1999-10-13. Applicant: Therapy Equipment, Inc.. Device class: 2.

Clearance details

Applicant: Therapy Equipment, Inc.
Product code: Code IKD
Device class: Class 2
Regulation: 21 CFR 890.1175
Advisory panel: Physical Medicine
Date received: 1999-07-15
Decision date: 1999-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Palm Beach, FL, 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.