LINEAR LIFT DEVICE— 510(k) K881676

Substantially Equivalent

Cybex

FDA 510(k) clearance K881676 for LINEAR LIFT DEVICE, Substantially Equivalent on 1990-04-25. Applicant: Cybex. Device class: 2.

Clearance details

Applicant: Cybex
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1988-04-19
Decision date: 1990-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ronkonkoma, 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.