POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE
K-Number: K082598 · 2009-01-07
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Device Summary
Frequently Asked Questions
What is the POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE?
POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2009-01-07. The listed applicant is Tangshan Zhonghong Pulin Group Co., Ltd.. The 510(k) number is K082598.
When did POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE receive FDA 510(k) clearance?
POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE received FDA 510(k) clearance on 2009-01-07, under 510(k) number K082598.
Who is the listed applicant for POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE?
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 POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE?
The FDA product code for POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE is LZA.
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: LZA)
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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