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FDA 510(k)

DYNAVISION 2000

K-Number: K911938 · 1991-08-02

ApplicantPerformance Ent.
Decision Date1991-08-02
Product CodeLQD
DecisionSubstantially Equivalent

Device Summary

DYNAVISION 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Performance Ent.. It received FDA 510(k) clearance on 1991-08-02 under 510(k) number K911938. The device is classified under product code LQD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNAVISION 2000?

DYNAVISION 2000 is a medical device that received FDA 510(k) clearance on 1991-08-02. The listed applicant is Performance Ent.. The 510(k) number is K911938.

When did DYNAVISION 2000 receive FDA 510(k) clearance?

DYNAVISION 2000 received FDA 510(k) clearance on 1991-08-02, under 510(k) number K911938.

Who is the listed applicant for DYNAVISION 2000?

The FDA 510(k) record lists Performance Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNAVISION 2000?

The FDA product code for DYNAVISION 2000 is LQD.

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Related Devices (Code: LQD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K173915Test of Variables of Attention (T.O.V.A.)The Tova CompanyK170082Test of Variables of Attention (T.O.V.A.) Version 9.0The Tova CompanyK143468QbCheckQbtech ABK122149QBTESQbtech ABK040894QBTESTQbtech ABK020800OPTAX SYSTEMOptax Systems, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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