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FDA 510(k)

MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM

K-Number: K891383 · 1989-06-01

ApplicantOxford Medilog, Inc.
Decision Date1989-06-01
Product CodeOLZ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM 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 1989-06-01 under 510(k) number K891383. The device is classified under product code OLZ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM?

MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1989-06-01. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K891383.

When did MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM receive FDA 510(k) clearance?

MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM received FDA 510(k) clearance on 1989-06-01, under 510(k) number K891383.

Who is the listed applicant for MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM?

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 9200 EEG REPLAY/ANALYSIS SYSTEM?

The FDA product code for MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM is OLZ.

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Other records listing Oxford Medilog, Inc. as applicant

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K923737MODEL MEDILOG RAPIDEK920295MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)K912890MODEL SONICAID AXISK912639SONICAID TEAMK904763MENTOR EEG SYSTEMK902690SONICAID MODEL MERIDIAN 800

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Related Devices (Code: OLZ)

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.

K253390SOMNUM (SOMNUM)Honeynaps Co., Ltd.K253668Onera SleepMap (SLEEPMAP)Onera B.V.K250851Hypnos (369054-200)Cadwell Industries, Inc.K252330DeepRESPNox Medical EhfK250058NEAT 001Brain Electrophysiology Laboratory Company, LLCK241960DeepRESPNox Medical Ehf

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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