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FDA 510(k)

PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH

K-Number: K002459 · 2000-11-08

ApplicantAgilent Technologies, Inc.
Decision Date2000-11-08
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 2000-11-08 under 510(k) number K002459. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH?

PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 2000-11-08. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K002459.

When did PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH receive FDA 510(k) clearance?

PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH received FDA 510(k) clearance on 2000-11-08, under 510(k) number K002459.

Who is the listed applicant for PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH?

The FDA 510(k) record lists Agilent Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH?

The FDA product code for PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPH is DPS.

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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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