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FDA 510(k)

PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A

K-Number: K874421 · 1988-01-28

ApplicantHewlett-Packard Co.
Decision Date1988-01-28
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A 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 1988-01-28 under 510(k) number K874421. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A?

PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K874421.

When did PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A receive FDA 510(k) clearance?

PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A received FDA 510(k) clearance on 1988-01-28, under 510(k) number K874421.

Who is the listed applicant for PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A?

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 PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A?

The FDA product code for PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A is DRX.

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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: DRX)

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.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing Co., Ltd.

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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