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FDA 510(k)

NIC-200 VENTRICULAR FUNCTION ANALYZER

K-Number: K792466 · 1980-01-24

ApplicantNicolet Biomedical Instruments
Decision Date1980-01-24
Product CodeDQC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NIC-200 VENTRICULAR FUNCTION ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical Instruments. It received FDA 510(k) clearance on 1980-01-24 under 510(k) number K792466. The device is classified under product code DQC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIC-200 VENTRICULAR FUNCTION ANALYZER?

NIC-200 VENTRICULAR FUNCTION ANALYZER is a medical device that received FDA 510(k) clearance on 1980-01-24. The listed applicant is Nicolet Biomedical Instruments. The 510(k) number is K792466.

When did NIC-200 VENTRICULAR FUNCTION ANALYZER receive FDA 510(k) clearance?

NIC-200 VENTRICULAR FUNCTION ANALYZER received FDA 510(k) clearance on 1980-01-24, under 510(k) number K792466.

Who is the listed applicant for NIC-200 VENTRICULAR FUNCTION ANALYZER?

The FDA 510(k) record lists Nicolet Biomedical Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIC-200 VENTRICULAR FUNCTION ANALYZER?

The FDA product code for NIC-200 VENTRICULAR FUNCTION ANALYZER is DQC.

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Other records listing Nicolet Biomedical Instruments 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.

K880573MODIFIED NICOLET VIKING SYSTEMK873736NICOLET DIGITAL TWO PIECE HEARING AIDK873964NICOLET DISPOSABLE PRASS PROBEK873535NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEMK871678NICOLET AMP 6R11 SYSTEMK862592PHOENIX SYSTEM SEVEN.

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Related Devices (Code: DQC)

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.

K950537CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPHCardiophonics, Inc.K952651LIFE SOUND SENSORFlowscan, Inc.K943726ACOUSTIC RECORDERTechnology Applications Assoc., Inc.K924054PHONOCARDIOGRAPHEcho UltrasoundK902185DYNAMIC SPECTRAL PHONOCARDIOGRAPHReeves Scientific, Inc.K900560ACUSON HEARTSOUND/PULSE/RESPIRATION MODULEAcuson Corp.

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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