Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALCATRON AND / OR MULTIPLE BRAND

K-Number: K112222 · 2011-10-27

Decision Date2011-10-27
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALCATRON AND / OR MULTIPLE BRAND is the device name listed in this FDA 510(k) record. The listed applicant is Alcatron Gloves Factory. It received FDA 510(k) clearance on 2011-10-27 under 510(k) number K112222. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

↑