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FDA 510(k)

CLINICAL GRAPHICS ANALYZER

K-Number: K780468 · 1978-06-19

ApplicantNumonics Corp.
Decision Date1978-06-19
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLINICAL GRAPHICS ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Numonics Corp.. It received FDA 510(k) clearance on 1978-06-19 under 510(k) number K780468. 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 CLINICAL GRAPHICS ANALYZER?

CLINICAL GRAPHICS ANALYZER is a medical device that received FDA 510(k) clearance on 1978-06-19. The listed applicant is Numonics Corp.. The 510(k) number is K780468.

When did CLINICAL GRAPHICS ANALYZER receive FDA 510(k) clearance?

CLINICAL GRAPHICS ANALYZER received FDA 510(k) clearance on 1978-06-19, under 510(k) number K780468.

Who is the listed applicant for CLINICAL GRAPHICS ANALYZER?

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

What is the FDA product code for CLINICAL GRAPHICS ANALYZER?

The FDA product code for CLINICAL GRAPHICS ANALYZER is DQK.

Related Clinical Trials

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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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