SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES
K-Number: K954381 · 1995-12-11
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Device Summary
Frequently Asked Questions
What is the SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES?
SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1995-12-11. The listed applicant is Shanghai Poseidon Plastic Products Co., Ltd.. The 510(k) number is K954381.
When did SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES receive FDA 510(k) clearance?
SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES received FDA 510(k) clearance on 1995-12-11, under 510(k) number K954381.
Who is the listed applicant for SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES?
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 SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES?
The FDA product code for SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM 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 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: 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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