ANATOMICAL EXAMINATION GLOVES
K-Number: K892579 · 1989-07-14
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Device Summary
Frequently Asked Questions
What is the ANATOMICAL EXAMINATION GLOVES?
ANATOMICAL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Ansell Pacific, Inc.. The 510(k) number is K892579.
When did ANATOMICAL EXAMINATION GLOVES receive FDA 510(k) clearance?
ANATOMICAL EXAMINATION GLOVES received FDA 510(k) clearance on 1989-07-14, under 510(k) number K892579.
Who is the listed applicant for ANATOMICAL EXAMINATION GLOVES?
The FDA 510(k) record lists Ansell Pacific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANATOMICAL EXAMINATION GLOVES?
The FDA product code for ANATOMICAL 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 Ansell Pacific, 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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