LATEX EXAMINATION GLOVES NON-STERILE
K-Number: K890356 · 1989-04-06
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Device Summary
Frequently Asked Questions
What is the LATEX EXAMINATION GLOVES NON-STERILE?
LATEX EXAMINATION GLOVES NON-STERILE is a medical device that received FDA 510(k) clearance on 1989-04-06. The listed applicant is Quest Intl., Inc.. The 510(k) number is K890356.
When did LATEX EXAMINATION GLOVES NON-STERILE receive FDA 510(k) clearance?
LATEX EXAMINATION GLOVES NON-STERILE received FDA 510(k) clearance on 1989-04-06, under 510(k) number K890356.
Who is the listed applicant for LATEX EXAMINATION GLOVES NON-STERILE?
The FDA 510(k) record lists Quest Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAMINATION GLOVES NON-STERILE?
The FDA product code for LATEX EXAMINATION GLOVES NON-STERILE 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 Quest Intl., Inc. 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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