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FDA 510(k)

CARDIOVUE ACCESSORY CART

K-Number: K820033 · 1982-01-22

ApplicantDiasonics, Inc.
Decision Date1982-01-22
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOVUE ACCESSORY CART is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K820033. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOVUE ACCESSORY CART?

CARDIOVUE ACCESSORY CART is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Diasonics, Inc.. The 510(k) number is K820033.

When did CARDIOVUE ACCESSORY CART receive FDA 510(k) clearance?

CARDIOVUE ACCESSORY CART received FDA 510(k) clearance on 1982-01-22, under 510(k) number K820033.

Who is the listed applicant for CARDIOVUE ACCESSORY CART?

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

What is the FDA product code for CARDIOVUE ACCESSORY CART?

The FDA product code for CARDIOVUE ACCESSORY CART is DSF.

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Other records listing Diasonics, Inc. 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.

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Related Devices (Code: DSF)

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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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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