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FDA 510(k)

ELECTROCARDIOCORDER RECORDER 453

K-Number: K833661 · 1983-11-28

ApplicantDel Mar Avionics
Decision Date1983-11-28
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTROCARDIOCORDER RECORDER 453 is the device name listed in this FDA 510(k) record. The listed applicant is Del Mar Avionics. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833661. 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 ELECTROCARDIOCORDER RECORDER 453?

ELECTROCARDIOCORDER RECORDER 453 is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Del Mar Avionics. The 510(k) number is K833661.

When did ELECTROCARDIOCORDER RECORDER 453 receive FDA 510(k) clearance?

ELECTROCARDIOCORDER RECORDER 453 received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833661.

Who is the listed applicant for ELECTROCARDIOCORDER RECORDER 453?

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

What is the FDA product code for ELECTROCARDIOCORDER RECORDER 453?

The FDA product code for ELECTROCARDIOCORDER RECORDER 453 is DSH.

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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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