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FDA 510(k)

HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR

K-Number: K950483 · 1995-05-22

ApplicantHewlett-Packard Co.
Decision Date1995-05-22
Product CodeDRO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR 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 1995-05-22 under 510(k) number K950483. 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 HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR?

HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR is a medical device that received FDA 510(k) clearance on 1995-05-22. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K950483.

When did HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR receive FDA 510(k) clearance?

HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR received FDA 510(k) clearance on 1995-05-22, under 510(k) number K950483.

Who is the listed applicant for HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR?

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 HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR?

The FDA product code for HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR is DRO.

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Other records listing Hewlett-Packard Co. as applicant

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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 ElectronicsK983232PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERTTz Medical, Inc.K983196PADTAK PACE/DEFIB/CARDIOVERT MONITORING ELECTRODE(S)Tz 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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