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FDA 510(k)

MEDILOG PH1

K-Number: K840934 · 1984-06-28

ApplicantOxford Medilog, Inc.
Decision Date1984-06-28
Product CodeEXW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDILOG PH1 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 1984-06-28 under 510(k) number K840934. The device is classified under product code EXW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG PH1?

MEDILOG PH1 is a medical device that received FDA 510(k) clearance on 1984-06-28. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K840934.

When did MEDILOG PH1 receive FDA 510(k) clearance?

MEDILOG PH1 received FDA 510(k) clearance on 1984-06-28, under 510(k) number K840934.

Who is the listed applicant for MEDILOG PH1?

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 PH1?

The FDA product code for MEDILOG PH1 is EXW.

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Other records listing Oxford Medilog, Inc. as applicant

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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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