REMUSK MP— 510(k) K922029

Name: FDA 510(k) clearance K922029
Creator: U.S. Food and Drug Administration
Published: 1992-10-06

Substantially Equivalent

Equipement Biomedical Specialise, Inc.

FDA 510(k) clearance K922029 for REMUSK MP, Substantially Equivalent on 1992-10-06. Applicant: Equipement Biomedical Specialise, Inc.. Device class: 2.

Clearance details

Applicant: Equipement Biomedical Specialise, Inc.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1992-05-01
Decision date: 1992-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code LBB

view all

K162412 — Hoggan Scientific® microFET22017-03-09
K073154 — FACTS HAND AND PINCH GRIP COMBO2008-02-14
K052309 — DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH50062005-09-27
K042889 — DYNAMOMETER - MODEL FCE AND MODEL MSC2004-11-16
K012492 — KADANCE 20002001-11-02

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