VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED
K-Number: K982257 · 1998-08-03
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Device Summary
Frequently Asked Questions
What is the VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED?
VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED is a medical device that received FDA 510(k) clearance on 1998-08-03. The listed applicant is Taian Plastics Products (Jingxing) Co., Ltd.. The 510(k) number is K982257.
When did VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED receive FDA 510(k) clearance?
VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED received FDA 510(k) clearance on 1998-08-03, under 510(k) number K982257.
Who is the listed applicant for VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED?
The FDA 510(k) record lists Taian Plastics Products (Jingxing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED?
The FDA product code for VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED 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 Taian Plastics Products (Jingxing) 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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