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FDA 510(k)

HEART-CHECK ECG TRANSMITTER

K-Number: K841875 · 1984-06-22

ApplicantPhysio Ventures, Inc.
Decision Date1984-06-22
Product Code
DecisionSubstantially Equivalent

Device Summary

HEART-CHECK ECG TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Physio Ventures, Inc.. It received FDA 510(k) clearance on 1984-06-22 under 510(k) number K841875. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEART-CHECK ECG TRANSMITTER?

HEART-CHECK ECG TRANSMITTER is a medical device that received FDA 510(k) clearance on 1984-06-22. The listed applicant is Physio Ventures, Inc.. The 510(k) number is K841875.

When did HEART-CHECK ECG TRANSMITTER receive FDA 510(k) clearance?

HEART-CHECK ECG TRANSMITTER received FDA 510(k) clearance on 1984-06-22, under 510(k) number K841875.

Who is the listed applicant for HEART-CHECK ECG TRANSMITTER?

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

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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.

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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.

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