Alko Diagnostic, Corporation
Our dedicated staff understands that quality is demanded by our customers. For this reason, ALKO is committed to a "Total Quality Process", ensuring constant focus and sensitivity to customer issues and requirements. This "Quality Process" is integrated throughout our organization. ALKO is regulated in the United States by the Food and Drug Administration (FDA). Therefore, it is essential that we strive to meet customer needs and comply with the Quality System Regulations set forth by the FDA.
ALKO products are designed to serve as direct replacements to those of the Original Equipment Manufacturer (OEM). Some products manufactured by ALKO require 510(k) clearance from the FDA. This clearance process includes time intensive correlation and precision studies, wherein ALKO products are compared to OEM products to determine substantial equivalence.
ALKO was founded with the purpose of providing premium quality laboratory consumables, of equal or higher quality, at a better value than the OEM. ALKO markets to over 4,000 laboratories in 60 countries worldwide. As budgets continue to tighten and healthcare reform remains a key issue, it is critical for laboratory decision makers to consider ALKO products and the many value added benefits we have to offer.
We realize that offering premium quality products is not the only expectation in today's market. That is why we support our customers 100%, by providing superior overall quality in our products, sales, service and support. Our knowledgeable telesales team and highly trained technical service staff work together to assist with product or instrument related issues. Join thousands of medical facilities worldwide and see why ALKO is "The Best Value Alternative for Blood Gas and ISE".