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FDA 510(k)

GOODNET

K-Number: K010763 · 2001-05-25

ApplicantGoodman Co., Ltd.
Decision Date2001-05-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GOODNET is the device name listed in this FDA 510(k) record. The listed applicant is Goodman Co., Ltd.. It received FDA 510(k) clearance on 2001-05-25 under 510(k) number K010763. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOODNET?

GOODNET is a medical device that received FDA 510(k) clearance on 2001-05-25. The listed applicant is Goodman Co., Ltd.. The 510(k) number is K010763.

When did GOODNET receive FDA 510(k) clearance?

GOODNET received FDA 510(k) clearance on 2001-05-25, under 510(k) number K010763.

Who is the listed applicant for GOODNET?

The FDA 510(k) record lists Goodman Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GOODNET?

The FDA product code for GOODNET is LLZ.

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Other records listing Goodman Co., Ltd. as applicant

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Official Source

View on FDA Database →

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

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