FDA 510(k)

ELECTROCARDIOGRAPH, AT-300 3 CHANNEL

K-Number: K790233 · 1979-02-08

ApplicantHealth Technology Laboratories, Inc.

Decision Date1979-02-08

Product CodeDPS

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ELECTROCARDIOGRAPH, AT-300 3 CHANNEL is the device name listed in this FDA 510(k) record. The listed applicant is Health Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K790233. 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 ELECTROCARDIOGRAPH, AT-300 3 CHANNEL?

ELECTROCARDIOGRAPH, AT-300 3 CHANNEL is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Health Technology Laboratories, Inc.. The 510(k) number is K790233.

When did ELECTROCARDIOGRAPH, AT-300 3 CHANNEL receive FDA 510(k) clearance?

ELECTROCARDIOGRAPH, AT-300 3 CHANNEL received FDA 510(k) clearance on 1979-02-08, under 510(k) number K790233.

Who is the listed applicant for ELECTROCARDIOGRAPH, AT-300 3 CHANNEL?

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

What is the FDA product code for ELECTROCARDIOGRAPH, AT-300 3 CHANNEL?

The FDA product code for ELECTROCARDIOGRAPH, AT-300 3 CHANNEL is DPS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.