ELECTRO-MYOSCOPE 85— 510(k) K833927

Name: FDA 510(k) clearance K833927
Creator: U.S. Food and Drug Administration
Published: 1983-12-27

Substantially Equivalent

Biomedical Design Instruments

FDA 510(k) clearance K833927 for ELECTRO-MYOSCOPE 85, Substantially Equivalent on 1983-12-27. Applicant: Biomedical Design Instruments. Device class: 2.

Clearance details

Applicant: Biomedical Design Instruments
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1983-11-14
Decision date: 1983-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKN

view all

K172743 — Natus VikingQuest2017-12-19
K163150 — ViMove22017-07-14
K162383 — Cadwell Sierra Summit, Cadwell Sierra Ascent2017-03-01
K142494 — ViMove2015-05-28
K131094 — VIMOVE2014-07-11

More clearances from Biomedical Design Instruments

view all

K883911 — ELECTRO-ACUSCOPE 851990-02-02
K833928 — MYOPULSE1984-12-14

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