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FDA 510(k)

DIGITAL HOLTER RECORDER

K-Number: K942781 · 1995-01-24

ApplicantAgilent Technologies
Decision Date1995-01-24
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL HOLTER RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies. It received FDA 510(k) clearance on 1995-01-24 under 510(k) number K942781. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL HOLTER RECORDER?

DIGITAL HOLTER RECORDER is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is Agilent Technologies. The 510(k) number is K942781.

When did DIGITAL HOLTER RECORDER receive FDA 510(k) clearance?

DIGITAL HOLTER RECORDER received FDA 510(k) clearance on 1995-01-24, under 510(k) number K942781.

Who is the listed applicant for DIGITAL HOLTER RECORDER?

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 DIGITAL HOLTER RECORDER?

The FDA product code for DIGITAL HOLTER RECORDER is DSH.

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Other records listing Agilent Technologies 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.

K0109492010 PLUS HOLTER FOR WINDOWSK0039402010 PLUS HOLTER FOR WINDOWSK0037632010 PLUS HOLTER FOR WINDOWSK001308MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEWK990093ZYMED TELEMETRY SYSTEM: MODEL EASIVIEWK980186ZYMED TELEMETRY SYSTEM

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Related Devices (Code: DSH)

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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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