VINYL PATIENT EXAMINATION GLOVES POWDER-FREE
K-Number: K973998 · 1997-11-18
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Device Summary
Frequently Asked Questions
What is the VINYL PATIENT EXAMINATION GLOVES POWDER-FREE?
VINYL PATIENT EXAMINATION GLOVES POWDER-FREE is a medical device that received FDA 510(k) clearance on 1997-11-18. The listed applicant is Everrise Glove Products Co., Ltd.. The 510(k) number is K973998.
When did VINYL PATIENT EXAMINATION GLOVES POWDER-FREE receive FDA 510(k) clearance?
VINYL PATIENT EXAMINATION GLOVES POWDER-FREE received FDA 510(k) clearance on 1997-11-18, under 510(k) number K973998.
Who is the listed applicant for VINYL PATIENT EXAMINATION GLOVES POWDER-FREE?
The FDA 510(k) record lists Everrise Glove Products 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 POWDER-FREE?
The FDA product code for VINYL PATIENT EXAMINATION GLOVES POWDER-FREE 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 Everrise Glove 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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