Hewlett-Packard GmbH is one of 238 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Hewlett-Packard GmbH - FDA 510(k) Cleared Devices
Recent clearances: HP VIRIDIA MULTI-MEASUREMENT SERVER/COMPACT PORTABLE PATIENT MONITOR MODELS M3000A, M3046A, M3015A, REL.B, HP VIRIDIA MULTI-MEASUREMENT SERVER/COMPACT PORTABLE PATIENT MONITOR M3000A/M3046A/M3016A,REL B, HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K WITH EASI-ST SEGMENT MEASUREMENT, HP VIRIDIA CMS 24/26, REV K WITH
Hewlett-Packard GmbH has 16 FDA 510(k) cleared medical devices. Based in 71004 Boblingen, DE.
Historical record: 16 cleared submissions from 1995 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hewlett-Packard GmbH Filter by specialty or product code using the sidebar.