RUBBER TREE BRAND
K-Number: K894214 · 1989-08-15
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement