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FDA 510(k)

KAO YING

K-Number: K946010 · 1995-03-07

ApplicantKao Ying Industrial Co., Ltd.
Decision Date1995-03-07
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KAO YING is the device name listed in this FDA 510(k) record. The listed applicant is Kao Ying Industrial Co., Ltd.. It received FDA 510(k) clearance on 1995-03-07 under 510(k) number K946010. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAO YING?

KAO YING is a medical device that received FDA 510(k) clearance on 1995-03-07. The listed applicant is Kao Ying Industrial Co., Ltd.. The 510(k) number is K946010.

When did KAO YING receive FDA 510(k) clearance?

KAO YING received FDA 510(k) clearance on 1995-03-07, under 510(k) number K946010.

Who is the listed applicant for KAO YING?

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

What is the FDA product code for KAO YING?

The FDA product code for KAO YING is LYZ.

Other records listing Kao Ying Industrial Co., Ltd. as applicant

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.

K892565PATIENT EXAMINATION GLOVE (VINYL)

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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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