PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG
K-Number: K891497 · 1989-07-31
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG?
PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG is a medical device that received FDA 510(k) clearance on 1989-07-31. The listed applicant is B.C. Young Intertrade Corp.. The 510(k) number is K891497.
When did PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG received FDA 510(k) clearance on 1989-07-31, under 510(k) number K891497.
Who is the listed applicant for PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG?
The FDA 510(k) record lists B.C. Young Intertrade Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG?
The FDA product code for PATIENT EXAM GLOVES (LATEX) MFG. HUA GUANG 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 B.C. Young Intertrade Corp. 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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