HI-RIDER WHEELCHAIR— 510(k) K890695

Substantially Equivalent

Retec USA, Inc.

FDA 510(k) clearance K890695 for HI-RIDER WHEELCHAIR, Substantially Equivalent on 1989-04-10. Applicant: Retec USA, Inc.. Device class: 2.

Clearance details

Applicant: Retec USA, Inc.
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 1989-02-10
Decision date: 1989-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orchard Park, NY, 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.