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FDA 510(k)

ZYMED HOLTER SCANNER MODEL 2010

K-Number: K930806 · 1994-04-25

ApplicantAgilent Technologies
Decision Date1994-04-25
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZYMED HOLTER SCANNER MODEL 2010 is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies. It received FDA 510(k) clearance on 1994-04-25 under 510(k) number K930806. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZYMED HOLTER SCANNER MODEL 2010?

ZYMED HOLTER SCANNER MODEL 2010 is a medical device that received FDA 510(k) clearance on 1994-04-25. The listed applicant is Agilent Technologies. The 510(k) number is K930806.

When did ZYMED HOLTER SCANNER MODEL 2010 receive FDA 510(k) clearance?

ZYMED HOLTER SCANNER MODEL 2010 received FDA 510(k) clearance on 1994-04-25, under 510(k) number K930806.

Who is the listed applicant for ZYMED HOLTER SCANNER MODEL 2010?

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

What is the FDA product code for ZYMED HOLTER SCANNER MODEL 2010?

The FDA product code for ZYMED HOLTER SCANNER MODEL 2010 is DQK.

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Other records listing Agilent Technologies as applicant

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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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