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FDA 510(k)

LA JOIE

K-Number: K000736 · 2000-08-08

ApplicantGoomi Ehwa, Inc.
Decision Date2000-08-08
Product CodeHED
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LA JOIE is the device name listed in this FDA 510(k) record. The listed applicant is Goomi Ehwa, Inc.. It received FDA 510(k) clearance on 2000-08-08 under 510(k) number K000736. The device is classified under product code HED. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LA JOIE?

LA JOIE is a medical device that received FDA 510(k) clearance on 2000-08-08. The listed applicant is Goomi Ehwa, Inc.. The 510(k) number is K000736.

When did LA JOIE receive FDA 510(k) clearance?

LA JOIE received FDA 510(k) clearance on 2000-08-08, under 510(k) number K000736.

Who is the listed applicant for LA JOIE?

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

What is the FDA product code for LA JOIE?

The FDA product code for LA JOIE is HED.

Related Devices (Code: HED)

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

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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