EDI 320— 510(k) K873599

Substantially Equivalent

Cybex

FDA 510(k) clearance K873599 for EDI 320, Substantially Equivalent on 1987-10-16. Applicant: Cybex. Device class: 1.

Clearance details

Applicant: Cybex
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1987-09-04
Decision date: 1987-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ronkonkoma, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQX

K011827 — ORTELIUS 8002001-08-28
K971079 — INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE1997-07-09
K962377 — 3D-SPINE1996-09-03
K961212 — SPINAL TOUCH1996-06-12
K954647 — INCLINOMETER1995-10-30

More clearances from Cybex

K950095 — CYBEX 7701995-06-21
K905525 — CYBEX 60001991-02-14
K881676 — LINEAR LIFT DEVICE1990-04-25
K881681 — CYBEX BACK TESTING AND REHABILITATION SYSTEM1990-04-25
K894154 — METABOLIC SYSTEMS1989-10-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.