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FDA 510(k)

RUBBER TREE BRAND

K-Number: K894214 · 1989-08-15

Decision Date1989-08-15
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RUBBER TREE BRAND is the device name listed in this FDA 510(k) record. The listed applicant is Jinmei International, Inc.. It received FDA 510(k) clearance on 1989-08-15 under 510(k) number K894214. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUBBER TREE BRAND?

RUBBER TREE BRAND is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Jinmei International, Inc.. The 510(k) number is K894214.

When did RUBBER TREE BRAND receive FDA 510(k) clearance?

RUBBER TREE BRAND received FDA 510(k) clearance on 1989-08-15, under 510(k) number K894214.

Who is the listed applicant for RUBBER TREE BRAND?

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

What is the FDA product code for RUBBER TREE BRAND?

The FDA product code for RUBBER TREE BRAND is LYY.

Related Clinical Trials

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.

Related Devices (Code: LYY)

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.

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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