
Hewlett-Packard Co.
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19091-XXXXX SER. OF GLASS CAPILLARY COL. is an FDA 510(k)-cleared medical device (K791893) manufactured by Hewlett-Packard Co.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 29, 1979. Regulation: 8.