CIR LATEX GLOVES
K-Number: K924419 · 1993-02-10
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Device Summary
Frequently Asked Questions
What is the CIR LATEX GLOVES?
CIR LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1993-02-10. The listed applicant is Crocker Industrial Resources Sdn. Bhd.. The 510(k) number is K924419.
When did CIR LATEX GLOVES receive FDA 510(k) clearance?
CIR LATEX GLOVES received FDA 510(k) clearance on 1993-02-10, under 510(k) number K924419.
Who is the listed applicant for CIR LATEX GLOVES?
The FDA 510(k) record lists Crocker Industrial Resources Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CIR LATEX GLOVES?
The FDA product code for CIR 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 Crocker Industrial Resources Sdn. Bhd. 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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