GLOVE, EXAMINATION, VINYL
K-Number: K952050 · 1996-08-12
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Device Summary
Frequently Asked Questions
What is the GLOVE, EXAMINATION, VINYL?
GLOVE, EXAMINATION, VINYL is a medical device that received FDA 510(k) clearance on 1996-08-12. The listed applicant is Oak Carolina, Inc.. The 510(k) number is K952050.
When did GLOVE, EXAMINATION, VINYL receive FDA 510(k) clearance?
GLOVE, EXAMINATION, VINYL received FDA 510(k) clearance on 1996-08-12, under 510(k) number K952050.
Who is the listed applicant for GLOVE, EXAMINATION, VINYL?
The FDA 510(k) record lists Oak Carolina, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLOVE, EXAMINATION, VINYL?
The FDA product code for GLOVE, EXAMINATION, VINYL 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 Oak Carolina, 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: 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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