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FDA 510(k)

ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE

K-Number: K900560 · 1990-12-03

ApplicantAcuson Corp.
Decision Date1990-12-03
Product CodeDQC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Corp.. It received FDA 510(k) clearance on 1990-12-03 under 510(k) number K900560. 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 ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE?

ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE is a medical device that received FDA 510(k) clearance on 1990-12-03. The listed applicant is Acuson Corp.. The 510(k) number is K900560.

When did ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE receive FDA 510(k) clearance?

ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE received FDA 510(k) clearance on 1990-12-03, under 510(k) number K900560.

Who is the listed applicant for ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE?

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

What is the FDA product code for ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE?

The FDA product code for ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE is DQC.

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Other records listing Acuson Corp. 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.

K023772KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEMK022896CSV12 SOFTWARE VIEWERK022567SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEMK021497CYPRESS ULTRASOUND SYSTEMK010950CYPRESS SYSTEMK0028073D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSING

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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.K900365PAG MICROPROCESSOR-CONTROLLED MODULELife Sciences Manufacturing, Inc.

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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