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FDA 510(k)

MODEL SONICAID AXIS

K-Number: K912890 · 1992-01-09

ApplicantOxford Medilog, Inc.
Decision Date1992-01-09
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL SONICAID AXIS 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 1992-01-09 under 510(k) number K912890. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL SONICAID AXIS?

MODEL SONICAID AXIS is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K912890.

When did MODEL SONICAID AXIS receive FDA 510(k) clearance?

MODEL SONICAID AXIS received FDA 510(k) clearance on 1992-01-09, under 510(k) number K912890.

Who is the listed applicant for MODEL SONICAID AXIS?

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 MODEL SONICAID AXIS?

The FDA product code for MODEL SONICAID AXIS is HGM.

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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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