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FDA 510(k)

DEL MAR AVIONICS MODEL 551 NEUROCORDER

K-Number: K822751 · 1982-10-08

ApplicantDel Mar Avionics
Decision Date1982-10-08
Product Code
DecisionSubstantially Equivalent

Device Summary

DEL MAR AVIONICS MODEL 551 NEUROCORDER 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 1982-10-08 under 510(k) number K822751. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEL MAR AVIONICS MODEL 551 NEUROCORDER?

DEL MAR AVIONICS MODEL 551 NEUROCORDER is a medical device that received FDA 510(k) clearance on 1982-10-08. The listed applicant is Del Mar Avionics. The 510(k) number is K822751.

When did DEL MAR AVIONICS MODEL 551 NEUROCORDER receive FDA 510(k) clearance?

DEL MAR AVIONICS MODEL 551 NEUROCORDER received FDA 510(k) clearance on 1982-10-08, under 510(k) number K822751.

Who is the listed applicant for DEL MAR AVIONICS MODEL 551 NEUROCORDER?

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

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Other records listing Del Mar Avionics 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.

K990027OMNICORDER, MODEL 464K971696SENTINEL RECORDER, MODELS 471/472K963174HOLTER DIGICORDER WITH PACER OPTION (MODEL 483)K950020HOLTER PACERCORDER(R)K942653HOLTER SSR DIGICORDER(TM)K922221SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM

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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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