POWDERED VINYL EXAMINATION GLOVES
K-Number: K122100 · 2013-08-22
Advertisement
Device Summary
Frequently Asked Questions
What is the POWDERED VINYL EXAMINATION GLOVES?
POWDERED VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2013-08-22. The listed applicant is Wang Tong Xinghua Co., Ltd.. The 510(k) number is K122100.
When did POWDERED VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDERED VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 2013-08-22, under 510(k) number K122100.
Who is the listed applicant for POWDERED VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Wang Tong Xinghua Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERED VINYL EXAMINATION GLOVES?
The FDA product code for POWDERED VINYL 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 Wang Tong Xinghua 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.
Advertisement