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FDA 510(k)

MEDILOG OPTIMA

K-Number: K896535 · 1990-01-18

ApplicantOxford Medilog, Inc.
Decision Date1990-01-18
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDILOG OPTIMA 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 1990-01-18 under 510(k) number K896535. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG OPTIMA?

MEDILOG OPTIMA is a medical device that received FDA 510(k) clearance on 1990-01-18. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K896535.

When did MEDILOG OPTIMA receive FDA 510(k) clearance?

MEDILOG OPTIMA received FDA 510(k) clearance on 1990-01-18, under 510(k) number K896535.

Who is the listed applicant for MEDILOG OPTIMA?

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 OPTIMA?

The FDA product code for MEDILOG OPTIMA is DSK.

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Other records listing Oxford Medilog, Inc. as applicant

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Related Devices (Code: DSK)

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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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