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FDA 510(k)

CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH

K-Number: K950537 · 1996-03-01

ApplicantCardiophonics, Inc.
Decision Date1996-03-01
Product CodeDQC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Cardiophonics, Inc.. It received FDA 510(k) clearance on 1996-03-01 under 510(k) number K950537. 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 CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH?

CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1996-03-01. The listed applicant is Cardiophonics, Inc.. The 510(k) number is K950537.

When did CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH receive FDA 510(k) clearance?

CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH received FDA 510(k) clearance on 1996-03-01, under 510(k) number K950537.

Who is the listed applicant for CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH?

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

What is the FDA product code for CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH?

The FDA product code for CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH is DQC.

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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.

K952651LIFE SOUND SENSORFlowscan, Inc.K943726ACOUSTIC RECORDERTechnology Applications Assoc., Inc.K924054PHONOCARDIOGRAPHEcho UltrasoundK902185DYNAMIC SPECTRAL PHONOCARDIOGRAPHReeves Scientific, Inc.K900560ACUSON HEARTSOUND/PULSE/RESPIRATION MODULEAcuson Corp.K900365PAG MICROPROCESSOR-CONTROLLED MODULELife Sciences Manufacturing, Inc.

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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