DYNAVISION 2000— 510(k) K911938

Substantially Equivalent

Performance Ent.

FDA 510(k) clearance K911938 for DYNAVISION 2000, Substantially Equivalent on 1991-08-02. Applicant: Performance Ent.. Device class: Unclassified.

Clearance details

Applicant: Performance Ent.
Product code: Code LQD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1991-05-01
Decision date: 1991-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, L3r 2a7, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code LQD

K173915 — Test of Variables of Attention (T.O.V.A.)2018-03-22
K170082 — Test of Variables of Attention (T.O.V.A.) Version 9.02017-05-17
K143468 — QbCheck2016-03-22
K141865 — DANA2014-10-15
K133382 — QB TEST2014-03-24

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