ECU 1218— 510(k) K840808

Substantially Equivalent

Rehab Technology, Inc.

FDA 510(k) clearance K840808 for ECU 1218, Substantially Equivalent on 1984-03-19. Applicant: Rehab Technology, Inc.. Device class: 2.

Clearance details

Applicant: Rehab Technology, Inc.
Product code: Code IQA
Device class: Class 2
Regulation: 21 CFR 890.3725
Advisory panel: Physical Medicine
Date received: 1984-02-24
Decision date: 1984-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IQA

K961306 — DELTATALKER WITH INFRARED1996-06-27
K953905 — IMPERIUM1995-11-21
K953937 — LIAISON COMPUTER ACCESS & ENVIRONMENTAL CONTROL SYSTEM1995-10-31
K943244 — DEUCE1995-09-11
K944585 — SCANNING DIRECTOR1995-02-21

More clearances from Rehab Technology, Inc.

K921084 — THE EXCELSIOR1992-04-07
K850313 — TELEVISION CONTROL OPTION 12191985-04-25
K850314 — TELEVISION CONTROL OPTION 12201985-04-25

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