DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES
K-Number: K033723 · 2004-02-24
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES?
DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2004-02-24. The listed applicant is Baoding Guanzhong Glove Co., Ltd.. The 510(k) number is K033723.
When did DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2004-02-24, under 510(k) number K033723.
Who is the listed applicant for DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Baoding Guanzhong Glove Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES?
The FDA product code for DISPOSABLE POWDERED 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 Baoding Guanzhong Glove 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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