ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)— 510(k) K922550

Name: FDA 510(k) clearance K922550
Creator: U.S. Food and Drug Administration
Published: 1992-12-10

Substantially Equivalent

Verimed Holdings, Inc.

FDA 510(k) clearance K922550 for ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM), Substantially Equivalent on 1992-12-10. Applicant: Verimed Holdings, Inc.. Device class: 1.

Clearance details

Applicant: Verimed Holdings, Inc.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1992-05-29
Decision date: 1992-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Lauderdale, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQX

view all

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 Verimed Holdings, Inc.

view all

K981277 — PERIFORM1998-11-20
K954127 — BIOFEEDBACK DEVICE1995-11-14
K951969 — MYOEXORCISER II FUAL1995-06-14
K930670 — PHYACTION 7871993-07-02
K913912 — VERIMED PERINEOMETER1992-06-16

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