POWDERED FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES
K-Number: K070041 · 2007-03-28
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Device Summary
Frequently Asked Questions
What is the POWDERED FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES?
POWDERED FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2007-03-28. The listed applicant is Shijiazhuang Lianhe Shunda Plastic Products Co., L. The 510(k) number is K070041.
When did POWDERED FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDERED FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2007-03-28, under 510(k) number K070041.
Who is the listed applicant for POWDERED FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Shijiazhuang Lianhe Shunda Plastic Products Co., L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERED FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES?
The FDA product code for POWDERED FREE (WHITE) 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 Shijiazhuang Lianhe Shunda Plastic Products Co., L 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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