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FDA 510(k)

SPIRAL SCALP ELECTRODE, 14499A

K-Number: K771553 · 1977-08-25

ApplicantHewlett-Packard Co.
Decision Date1977-08-25
Product CodeHGP
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SPIRAL SCALP ELECTRODE, 14499A 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 1977-08-25 under 510(k) number K771553. The device is classified under product code HGP. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIRAL SCALP ELECTRODE, 14499A?

SPIRAL SCALP ELECTRODE, 14499A is a medical device that received FDA 510(k) clearance on 1977-08-25. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K771553.

When did SPIRAL SCALP ELECTRODE, 14499A receive FDA 510(k) clearance?

SPIRAL SCALP ELECTRODE, 14499A received FDA 510(k) clearance on 1977-08-25, under 510(k) number K771553.

Who is the listed applicant for SPIRAL SCALP ELECTRODE, 14499A?

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 SPIRAL SCALP ELECTRODE, 14499A?

The FDA product code for SPIRAL SCALP ELECTRODE, 14499A is HGP.

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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: HGP)

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.

K243291Goldtrace Fetal Spiral Electrode (FSE) (CNS000004)Neoventa Medical ABK030691FETAL SPIRAL ELECTRODE, MODEL FSE07000Clinical Innovations, Inc.K003458SOFT BEAT FETAL HEART RATE ELECTRODE MODEL SBT-7000Clinical Innovations, Inc.K943732LIFE TRACE FETAL SPIRAL ELECTRODE WITH MATERNAL REFERENCEGraphic Controls Corp.K910815CR SPIRAL ELECTRODENeward Enterprises, Inc.K911657FETAL SCALP SPIRAL ELECTRODEAdvanced Medical 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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