PATIENT EXAMINATION GLOES
K-Number: K102840 · 2011-02-18
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAMINATION GLOES?
PATIENT EXAMINATION GLOES is a medical device that received FDA 510(k) clearance on 2011-02-18. The listed applicant is Thai Hua Holding Co., Ltd.. The 510(k) number is K102840.
When did PATIENT EXAMINATION GLOES receive FDA 510(k) clearance?
PATIENT EXAMINATION GLOES received FDA 510(k) clearance on 2011-02-18, under 510(k) number K102840.
Who is the listed applicant for PATIENT EXAMINATION GLOES?
The FDA 510(k) record lists Thai Hua Holding Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAMINATION GLOES?
The FDA product code for PATIENT EXAMINATION GLOES 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.
Other records listing Thai Hua Holding 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.
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.
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