
Diagnostic Products Corp.
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SPECIFIC ALLERGEN MODULES FOR ALASTAT(TM) IGE SYS. is an FDA 510(k)-cleared medical device (K881899) manufactured by Diagnostic Products Corp.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 9, 1988. Regulation: 8.