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FDA 510(k)

MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)

K-Number: K920295 · 1992-08-18

ApplicantOxford Medilog, Inc.
Decision Date1992-08-18
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED) is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1992-08-18 under 510(k) number K920295. 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 MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)?

MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED) is a medical device that received FDA 510(k) clearance on 1992-08-18. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K920295.

When did MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED) receive FDA 510(k) clearance?

MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED) received FDA 510(k) clearance on 1992-08-18, under 510(k) number K920295.

Who is the listed applicant for MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)?

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

What is the FDA product code for MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)?

The FDA product code for MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED) is DQK.

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Other records listing Oxford Medilog, Inc. as applicant

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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

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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