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FDA 510(k)

MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION

K-Number: K895793 · 1990-02-13

ApplicantDel Mar Avionics
Decision Date1990-02-13
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION 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 1990-02-13 under 510(k) number K895793. 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 MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION?

MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION is a medical device that received FDA 510(k) clearance on 1990-02-13. The listed applicant is Del Mar Avionics. The 510(k) number is K895793.

When did MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION receive FDA 510(k) clearance?

MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION received FDA 510(k) clearance on 1990-02-13, under 510(k) number K895793.

Who is the listed applicant for MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION?

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 MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION?

The FDA product code for MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION is DSH.

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Other records listing Del Mar Avionics as applicant

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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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Related Devices (Code: DSH)

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.

K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens Co., Ltd.

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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