POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE
K-Number: K101594 · 2010-10-08
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Device Summary
Frequently Asked Questions
What is the POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE?
POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE is a medical device that received FDA 510(k) clearance on 2010-10-08. The listed applicant is Better Care Plastic Technology Cp., Ltd.. The 510(k) number is K101594.
When did POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE receive FDA 510(k) clearance?
POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE received FDA 510(k) clearance on 2010-10-08, under 510(k) number K101594.
Who is the listed applicant for POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE?
The FDA 510(k) record lists Better Care Plastic Technology Cp., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE?
The FDA product code for POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE 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 Better Care Plastic Technology Cp., 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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