MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO— 510(k) K873659

Name: FDA 510(k) clearance K873659
Creator: U.S. Food and Drug Administration
Published: 1988-04-21

Substantially Equivalent

Universal Gym Equipment, Inc.

FDA 510(k) clearance K873659 for MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO, Substantially Equivalent on 1988-04-21. Applicant: Universal Gym Equipment, Inc.. Device class: 2.

Clearance details

Applicant: Universal Gym Equipment, Inc.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1987-09-10
Decision date: 1988-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKK

view all

K123746 — AMES THERAPY DEVICE2013-05-24
K952090 — HUMAC SYSTEM1995-12-11
K951770 — BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP1995-11-16
K951916 — CC RIDER, MODEL ME1801995-10-04
K950095 — CYBEX 7701995-06-21

More clearances from Universal Gym Equipment, Inc.

view all

K873658 — ANKLE REFLEX TREATMENT UNIT (ARTU)1988-04-21

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