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FDA 510(k)

HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A

K-Number: K992636 · 1999-08-31

ApplicantHewlett-Packard Co.
Decision Date1999-08-31
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1999-08-31 under 510(k) number K992636. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A?

HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A is a medical device that received FDA 510(k) clearance on 1999-08-31. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K992636.

When did HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A receive FDA 510(k) clearance?

HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A received FDA 510(k) clearance on 1999-08-31, under 510(k) number K992636.

Who is the listed applicant for HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A?

The FDA product code for HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A is DXJ.

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Other records listing Hewlett-Packard Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K992543HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLEK993587HP M2376A DEVICE LINK SYSTEMK993169MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810AK992977HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504AK993516HP M2600A VIRIDIA TELEMETRY SYSTEMK993171HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A

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Related Devices (Code: DXJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K212003ESSENZ Patient MonitorLivanova Deutschland, GmbHK212208Philips IntelliVue GuardianSoftware (Rev. E.0X)Philips Medizin Systeme Boeblingen GmbHK201162Essence 55SP Large Monitor SystemShenyang Torch-Bigtide Digital Technology Co., Ltd.K173107Vios Central Station Monitor Software, Vios Central Server SoftwareVios Medical, Inc.K180534Philips IntelliVue GuardianSoftwarePhilips Medizin Systeme Boeblingen GmbHK173381Nexxis ORBarco N.V.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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