SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES
K-Number: K983645 · 1998-12-04
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Device Summary
Frequently Asked Questions
What is the SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES?
SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1998-12-04. The listed applicant is Shijiazhuang Great Eagle Plastic Products Co., Ltd.. The 510(k) number is K983645.
When did SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1998-12-04, under 510(k) number K983645.
Who is the listed applicant for SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Shijiazhuang Great Eagle Plastic Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES?
The FDA product code for SYNTHETIC POWDERED VINYL PATIENT 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 Shijiazhuang Great Eagle 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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