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FDA 510(k)

ANALYZER, MEDILOG II

K-Number: K790287 · 1979-02-28

ApplicantOxford Medilog, Inc.
Decision Date1979-02-28
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANALYZER, MEDILOG II 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 1979-02-28 under 510(k) number K790287. 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 ANALYZER, MEDILOG II?

ANALYZER, MEDILOG II is a medical device that received FDA 510(k) clearance on 1979-02-28. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K790287.

When did ANALYZER, MEDILOG II receive FDA 510(k) clearance?

ANALYZER, MEDILOG II received FDA 510(k) clearance on 1979-02-28, under 510(k) number K790287.

Who is the listed applicant for ANALYZER, MEDILOG II?

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 ANALYZER, MEDILOG II?

The FDA product code for ANALYZER, MEDILOG II is 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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