ALCATRON AND / OR MULTIPLE BRAND
K-Number: K112222 · 2011-10-27
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Device Summary
Frequently Asked Questions
What is the ALCATRON AND / OR MULTIPLE BRAND?
ALCATRON AND / OR MULTIPLE BRAND is a medical device that received FDA 510(k) clearance on 2011-10-27. The listed applicant is Alcatron Gloves Factory. The 510(k) number is K112222.
When did ALCATRON AND / OR MULTIPLE BRAND receive FDA 510(k) clearance?
ALCATRON AND / OR MULTIPLE BRAND received FDA 510(k) clearance on 2011-10-27, under 510(k) number K112222.
Who is the listed applicant for ALCATRON AND / OR MULTIPLE BRAND?
The FDA 510(k) record lists Alcatron Gloves Factory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALCATRON AND / OR MULTIPLE BRAND?
The FDA product code for ALCATRON AND / OR MULTIPLE BRAND is LYZ.
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 Alcatron Gloves Factory 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: LYZ)
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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