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FDA 510(k)

MULTIVARIATE DIGITAL CARDIOGRAPH

K-Number: K840875 · 1984-07-06

ApplicantClinical Microsystems Intl.
Decision Date1984-07-06
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTIVARIATE DIGITAL CARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Microsystems Intl.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K840875. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIVARIATE DIGITAL CARDIOGRAPH?

MULTIVARIATE DIGITAL CARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Clinical Microsystems Intl.. The 510(k) number is K840875.

When did MULTIVARIATE DIGITAL CARDIOGRAPH receive FDA 510(k) clearance?

MULTIVARIATE DIGITAL CARDIOGRAPH received FDA 510(k) clearance on 1984-07-06, under 510(k) number K840875.

Who is the listed applicant for MULTIVARIATE DIGITAL CARDIOGRAPH?

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

What is the FDA product code for MULTIVARIATE DIGITAL CARDIOGRAPH?

The FDA product code for MULTIVARIATE DIGITAL CARDIOGRAPH is DQK.

Related Clinical Trials

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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Other records listing Clinical Microsystems Intl. 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.

K801894RESPONDER II

Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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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