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FDA 510(k)

HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02

K-Number: K982619 · 1998-08-12

ApplicantHewlett-Packard Co.
Decision Date1998-08-12
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02 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 1998-08-12 under 510(k) number K982619. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02?

HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02 is a medical device that received FDA 510(k) clearance on 1998-08-12. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K982619.

When did HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02 receive FDA 510(k) clearance?

HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02 received FDA 510(k) clearance on 1998-08-12, under 510(k) number K982619.

Who is the listed applicant for HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02?

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 ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02?

The FDA product code for HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02 is CCL.

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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: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, 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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