UNIJECT EXAMINATION GLOVES
K-Number: K970191 · 1997-07-03
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Device Summary
Frequently Asked Questions
What is the UNIJECT EXAMINATION GLOVES?
UNIJECT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Uniject Gloves , Ltd.. The 510(k) number is K970191.
When did UNIJECT EXAMINATION GLOVES receive FDA 510(k) clearance?
UNIJECT EXAMINATION GLOVES received FDA 510(k) clearance on 1997-07-03, under 510(k) number K970191.
Who is the listed applicant for UNIJECT EXAMINATION GLOVES?
The FDA 510(k) record lists Uniject Gloves , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIJECT EXAMINATION GLOVES?
The FDA product code for UNIJECT EXAMINATION GLOVES is LYY.
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 Uniject Gloves , 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: LYY)
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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