PREPOWDER VINYL PATIENT EXAMINATION GLOVES
K-Number: K962026 · 1996-09-10
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Device Summary
Frequently Asked Questions
What is the PREPOWDER VINYL PATIENT EXAMINATION GLOVES?
PREPOWDER VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1996-09-10. The listed applicant is Hong Huang Tang Industrial Co., Ltd.. The 510(k) number is K962026.
When did PREPOWDER VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
PREPOWDER VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1996-09-10, under 510(k) number K962026.
Who is the listed applicant for PREPOWDER VINYL PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Hong Huang Tang Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREPOWDER VINYL PATIENT EXAMINATION GLOVES?
The FDA product code for PREPOWDER VINYL PATIENT EXAMINATION GLOVES is LYZ.
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 Hong Huang Tang 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.
Related Devices (Code: LYZ)
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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