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FDA 510(k)

MEDILOG EXCEL ECG ANALYSIS SYSTEM

K-Number: K885256 · 1989-05-31

ApplicantOxford Medical, Inc.
Decision Date1989-05-31
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDILOG EXCEL ECG ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medical, Inc.. It received FDA 510(k) clearance on 1989-05-31 under 510(k) number K885256. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG EXCEL ECG ANALYSIS SYSTEM?

MEDILOG EXCEL ECG ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is Oxford Medical, Inc.. The 510(k) number is K885256.

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

MEDILOG EXCEL ECG ANALYSIS SYSTEM received FDA 510(k) clearance on 1989-05-31, under 510(k) number K885256.

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

The FDA 510(k) record lists Oxford Medical, 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?

The FDA product code for MEDILOG EXCEL ECG ANALYSIS SYSTEM is DSI.

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 Oxford Medical, 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.

K951128MEDILOG STRESSLINK

Related Devices (Code: DSI)

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.

K243349BodyGuardian Remote Monitoring System (BGRMS v3.0)Boston Scientific Cardiac Diagnostic Technologies, Inc.K250356MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)Infobionic, Inc.K240177Zio AT® device (A100A1001)iRhythm Technologies, Inc.K230265MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemInfobionic, Inc.K231276SmartCardia 7L PlatformSmartcardia SAK193104Unified Arrhythmia Diagnostic System PocketECG IVMedicalgorithmics S.A.

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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