JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES
K-Number: K964800 · 1997-02-14
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Device Summary
Frequently Asked Questions
What is the JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES?
JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1997-02-14. The listed applicant is Shanghai Jiawang Industrial Co. , Ltd.. The 510(k) number is K964800.
When did JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 1997-02-14, under 510(k) number K964800.
Who is the listed applicant for JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Shanghai Jiawang Industrial Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JIAWANG PRE-POWDERED VINYL EXAMINATION GLOVES?
The FDA product code for JIAWANG PRE-POWDERED VINYL 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 Shanghai Jiawang Industrial 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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