NON-STERILE E.P. LATEX EXAMINATION GLOVE
K-Number: K982453 · 1998-11-30
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Device Summary
Frequently Asked Questions
What is the NON-STERILE E.P. LATEX EXAMINATION GLOVE?
NON-STERILE E.P. LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1998-11-30. The listed applicant is Ansell Perry. The 510(k) number is K982453.
When did NON-STERILE E.P. LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?
NON-STERILE E.P. LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1998-11-30, under 510(k) number K982453.
Who is the listed applicant for NON-STERILE E.P. LATEX EXAMINATION GLOVE?
The FDA 510(k) record lists Ansell Perry as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-STERILE E.P. LATEX EXAMINATION GLOVE?
The FDA product code for NON-STERILE E.P. LATEX EXAMINATION GLOVE 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 Ansell Perry 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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