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FDA 510(k)

HP M2376A DEVICE LINK SYSTEM

K-Number: K984194 · 1999-04-30

ApplicantHewlett-Packard Co.
Decision Date1999-04-30
Product CodeMQS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HP M2376A DEVICE LINK SYSTEM 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 1999-04-30 under 510(k) number K984194. The device is classified under product code MQS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP M2376A DEVICE LINK SYSTEM?

HP M2376A DEVICE LINK SYSTEM is a medical device that received FDA 510(k) clearance on 1999-04-30. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K984194.

When did HP M2376A DEVICE LINK SYSTEM receive FDA 510(k) clearance?

HP M2376A DEVICE LINK SYSTEM received FDA 510(k) clearance on 1999-04-30, under 510(k) number K984194.

Who is the listed applicant for HP M2376A DEVICE LINK SYSTEM?

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 M2376A DEVICE LINK SYSTEM?

The FDA product code for HP M2376A DEVICE LINK SYSTEM is MQS.

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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: MQS)

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.

K232283PhySoftAMS®Physician Software Systems, LLCK180410Dosis SAMDosis, Inc.K130579PHYSOFT AMSPhysicians Software Systems, LLCK042566VASC-ALERTVasc-Alert, Inc.K022963TRANSONIC SYRINGE WARMER, MODEL SYR-1000Transonic Systems, Inc.K021571TRANSONIC FLOW-QC SET MODEL ADT1010Transonic Systems, Inc.

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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