VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR
K-Number: K091770 · 2010-04-06
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Device Summary
Frequently Asked Questions
What is the VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR?
VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR is a medical device that received FDA 510(k) clearance on 2010-04-06. The listed applicant is Shijiazhuang Huijingyuan Plastic Co, Ltd.. The 510(k) number is K091770.
When did VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR receive FDA 510(k) clearance?
VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR received FDA 510(k) clearance on 2010-04-06, under 510(k) number K091770.
Who is the listed applicant for VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR?
The FDA 510(k) record lists Shijiazhuang Huijingyuan Plastic Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR?
The FDA product code for VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR 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 Huijingyuan Plastic 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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