BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES
K-Number: K022091 · 2002-12-30
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Device Summary
Frequently Asked Questions
What is the BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES?
BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2002-12-30. The listed applicant is Tangshan Zhonghong Pulin Group Co., Ltd.. The 510(k) number is K022091.
When did BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES receive FDA 510(k) clearance?
BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES received FDA 510(k) clearance on 2002-12-30, under 510(k) number K022091.
Who is the listed applicant for BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES?
The FDA 510(k) record lists Tangshan Zhonghong Pulin Group Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES?
The FDA product code for BALDUR BRAND VINYL POWDER-FREE 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 Tangshan Zhonghong Pulin Group 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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