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FDA 510(k)

MODELS M1722A, M1723A, M1724A DEFIBRILLATORS

K-Number: K915757 · 1992-07-30

ApplicantHewlett-Packard Co.
Decision Date1992-07-30
Product CodeDRO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODELS M1722A, M1723A, M1724A DEFIBRILLATORS 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 1992-07-30 under 510(k) number K915757. The device is classified under product code DRO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODELS M1722A, M1723A, M1724A DEFIBRILLATORS?

MODELS M1722A, M1723A, M1724A DEFIBRILLATORS is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K915757.

When did MODELS M1722A, M1723A, M1724A DEFIBRILLATORS receive FDA 510(k) clearance?

MODELS M1722A, M1723A, M1724A DEFIBRILLATORS received FDA 510(k) clearance on 1992-07-30, under 510(k) number K915757.

Who is the listed applicant for MODELS M1722A, M1723A, M1724A DEFIBRILLATORS?

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 MODELS M1722A, M1723A, M1724A DEFIBRILLATORS?

The FDA product code for MODELS M1722A, M1723A, M1724A DEFIBRILLATORS is DRO.

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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: DRO)

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.

K012404K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85Katecho, Inc.K012218LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODESThe Ludlow Company LPK000660ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413Medical Data ElectronicsK983196PADTAK PACE/DEFIB/CARDIOVERT MONITORING ELECTRODE(S)Tz Medical, Inc.K983232PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERTTz Medical, Inc.K974034PORTABLE INTENSIVE CARE UNITMedical Research Laboratories, 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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