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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Hewlett-Packard GmbH — Predicate Candidate Screening

16 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

127 daysmedian FDA review time
262 days90th percentile
16clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K993383HP VIRIDIA MULTI-MEASUREMENT SERVER/COMPACT PORTABLE PATIENTHewlett-Packard GmbH2000-02-031181
K992273HP VIRIDIA MULTI-MEASUREMENT SERVER/COMPACT PORTABLE PATIENTHewlett-Packard GmbH2000-01-282050
K992595HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K WITH EAHewlett-Packard GmbH1999-12-081270
K992674HP VIRIDIA CMS PATIENT MONITOR WITH EEG PARAMETER, MODEL M10Hewlett-Packard GmbH1999-11-08900
K990476HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26Hewlett-Packard GmbH1999-07-221560
K991773HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26Hewlett-Packard GmbH1999-06-07130
K990972HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26Hewlett-Packard GmbH1999-04-19270
K990125HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. KHewlett-Packard GmbH1999-01-29160
K981576MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL MHewlett-Packard GmbH1998-07-17740
K971910MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A)Hewlett-Packard GmbH1998-03-233040
K973437HEWLETT-PACKARD MODELS M1001B ECG M1002B ECG/RESPIRATION PLUHewlett-Packard GmbH1997-12-03840
K970456HEWLETT APCKARD SERIES 50 OB TRACEVUE OBSTETRICAL SURVEILLANHewlett-Packard GmbH1997-10-032390
K965160HP ORVUE INTRA-OP (M2510A)Hewlett-Packard GmbH1997-09-112620
K954351SERIES 50XMHewlett-Packard GmbH1996-03-081720
K951127HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULEHewlett-Packard GmbH1995-03-24110
K942842HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULEHewlett-Packard GmbH1995-02-162450

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda