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FDA 510(k)

MEDILOG 2500 SYSTEM

K-Number: K860078 · 1986-02-26

ApplicantOxford Medilog, Inc.
Decision Date1986-02-26
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDILOG 2500 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 1986-02-26 under 510(k) number K860078. 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 2500 SYSTEM?

MEDILOG 2500 SYSTEM is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K860078.

When did MEDILOG 2500 SYSTEM receive FDA 510(k) clearance?

MEDILOG 2500 SYSTEM received FDA 510(k) clearance on 1986-02-26, under 510(k) number K860078.

Who is the listed applicant for MEDILOG 2500 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 2500 SYSTEM?

The FDA product code for MEDILOG 2500 SYSTEM is DSI.

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Other records listing Oxford Medilog, Inc. as applicant

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Related Devices (Code: DSI)

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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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