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FDA 510(k)

OPTAX SYSTEM

K-Number: K020800 · 2002-06-10

ApplicantOptax Systems, Inc.
Decision Date2002-06-10
Product CodeLQD
DecisionSubstantially Equivalent

Device Summary

OPTAX SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Optax Systems, Inc.. It received FDA 510(k) clearance on 2002-06-10 under 510(k) number K020800. The device is classified under product code LQD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTAX SYSTEM?

OPTAX SYSTEM is a medical device that received FDA 510(k) clearance on 2002-06-10. The listed applicant is Optax Systems, Inc.. The 510(k) number is K020800.

When did OPTAX SYSTEM receive FDA 510(k) clearance?

OPTAX SYSTEM received FDA 510(k) clearance on 2002-06-10, under 510(k) number K020800.

Who is the listed applicant for OPTAX SYSTEM?

The FDA 510(k) record lists Optax Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPTAX SYSTEM?

The FDA product code for OPTAX SYSTEM 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.

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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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