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FDA 510(k)

SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING SYSTEM

K-Number: K943389 · 1995-03-17

ApplicantHewlett-Packard Co.
Decision Date1995-03-17
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING 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 1995-03-17 under 510(k) number K943389. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING SYSTEM?

SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1995-03-17. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K943389.

When did SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING SYSTEM receive FDA 510(k) clearance?

SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING SYSTEM received FDA 510(k) clearance on 1995-03-17, under 510(k) number K943389.

Who is the listed applicant for SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING 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 SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING SYSTEM?

The FDA product code for SIDESTREAM PUMP PLUG-IN MODULE OF COMPONENT MONITORING SYSTEM is CCK.

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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: CCK)

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.

K251641GF-310R Multigas Unit (GF-310R)Nihon Kohden CorporationK261633VisuBreathAffirm Medical Technologies II, LLCK253030Capnostream™35 Portable Respiratory Monitor (PM35MN)Covidien, LLCK250148Medical Gas Analyzer (AG200)Prior Care Science Technology, Ltd.K243956TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)Nihon Kohden CorporationK2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineBarbaras Development, 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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