BLASTOMERE BIOPSY PIPETTES, POLAR BODY BIOPSY PIPETTES

BLASTOMERE BIOPSY PIPETTES, POLAR BODY BIOPSY PIPETTES is an FDA 510(k)-cleared medical device (K092554) manufactured by Sunlight Medical, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 29, 2010. Regulation: 8.