CURITY DISPOSABLE LATEX GLOVES
K-Number: K891255 · 1989-04-13
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Device Summary
Frequently Asked Questions
What is the CURITY DISPOSABLE LATEX GLOVES?
CURITY DISPOSABLE LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-13. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K891255.
When did CURITY DISPOSABLE LATEX GLOVES receive FDA 510(k) clearance?
CURITY DISPOSABLE LATEX GLOVES received FDA 510(k) clearance on 1989-04-13, under 510(k) number K891255.
Who is the listed applicant for CURITY DISPOSABLE LATEX GLOVES?
The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURITY DISPOSABLE LATEX GLOVES?
The FDA product code for CURITY DISPOSABLE LATEX 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 Kendall Healthcare Products Co. Div.Of Tyco Health 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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