NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE
K-Number: K001836 · 2000-07-26
Advertisement
Device Summary
Frequently Asked Questions
What is the NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE?
NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE is a medical device that received FDA 510(k) clearance on 2000-07-26. The listed applicant is Shanghai Poseidon Plastic Products Co., Ltd.. The 510(k) number is K001836.
When did NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE receive FDA 510(k) clearance?
NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE received FDA 510(k) clearance on 2000-07-26, under 510(k) number K001836.
Who is the listed applicant for NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE?
The FDA 510(k) record lists Shanghai Poseidon Plastic Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE?
The FDA product code for NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE 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 Shanghai Poseidon Plastic Products 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: 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.
Advertisement