510(k) K791893

19091-XXXXX SER. OF GLASS CAPILLARY COL. by Hewlett-Packard Co. — Product Code DII

K791893 is an FDA 510(k) premarket notification submitted by Hewlett-Packard Co. for the device "19091-XXXXX SER. OF GLASS CAPILLARY COL.". The FDA issued a decision of Substantially Equivalent on October 30, 1979. The device falls under product code DII (Columns, Glc), a Class I device regulated under 21 CFR 862.2250. Hewlett-Packard Co. has at least 10 other 510(k) clearances on record.