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FDA 510(k)

MEDILOG 9000 SYSTEM

K-Number: K830295 · 1983-03-24

ApplicantOxford Medilog, Inc.
Decision Date1983-03-24
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDILOG 9000 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 1983-03-24 under 510(k) number K830295. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG 9000 SYSTEM?

MEDILOG 9000 SYSTEM is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K830295.

When did MEDILOG 9000 SYSTEM receive FDA 510(k) clearance?

MEDILOG 9000 SYSTEM received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830295.

Who is the listed applicant for MEDILOG 9000 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 9000 SYSTEM?

The FDA product code for MEDILOG 9000 SYSTEM is GWQ.

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Other records listing Oxford Medilog, Inc. as applicant

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Related Devices (Code: GWQ)

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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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