LATEX EXAM GLOVES (SURGICAL TYPE GLOVE)
K-Number: K892168 · 1989-07-14
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Device Summary
Frequently Asked Questions
What is the LATEX EXAM GLOVES (SURGICAL TYPE GLOVE)?
LATEX EXAM GLOVES (SURGICAL TYPE GLOVE) is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Hands-On Packaging , Ltd.. The 510(k) number is K892168.
When did LATEX EXAM GLOVES (SURGICAL TYPE GLOVE) receive FDA 510(k) clearance?
LATEX EXAM GLOVES (SURGICAL TYPE GLOVE) received FDA 510(k) clearance on 1989-07-14, under 510(k) number K892168.
Who is the listed applicant for LATEX EXAM GLOVES (SURGICAL TYPE GLOVE)?
The FDA 510(k) record lists Hands-On Packaging , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAM GLOVES (SURGICAL TYPE GLOVE)?
The FDA product code for LATEX EXAM GLOVES (SURGICAL TYPE 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 Hands-On Packaging , 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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