CYBEX BACK TESTING AND REHABILITATION SYSTEM— 510(k) K881681

Name: FDA 510(k) clearance K881681
Creator: U.S. Food and Drug Administration
Published: 1990-04-25

Substantially Equivalent

Cybex

FDA 510(k) clearance K881681 for CYBEX BACK TESTING AND REHABILITATION SYSTEM, 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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