PRIME PROTECTION POWDERED VINYL EXAMINATION GLOVES
K-Number: K070519 · 2007-04-10
Advertisement
Device Summary
Frequently Asked Questions
What is the PRIME PROTECTION POWDERED VINYL EXAMINATION GLOVES?
PRIME PROTECTION POWDERED VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2007-04-10. The listed applicant is Zhang Jia Gang Huayuan Plastic Co. , Ltd.. The 510(k) number is K070519.
When did PRIME PROTECTION POWDERED VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
PRIME PROTECTION POWDERED VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 2007-04-10, under 510(k) number K070519.
Who is the listed applicant for PRIME PROTECTION POWDERED VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Zhang Jia Gang Huayuan Plastic Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRIME PROTECTION POWDERED VINYL EXAMINATION GLOVES?
The FDA product code for PRIME PROTECTION 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 Zhang Jia Gang Huayuan 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.
Advertisement