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FDA 510(k)

SONICAID ONE

K-Number: K023618 · 2003-01-22

ApplicantOxford Instruments Medical , Ltd.
Decision Date2003-01-22
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SONICAID ONE is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Instruments Medical , Ltd.. It received FDA 510(k) clearance on 2003-01-22 under 510(k) number K023618. 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 SONICAID ONE?

SONICAID ONE is a medical device that received FDA 510(k) clearance on 2003-01-22. The listed applicant is Oxford Instruments Medical , Ltd.. The 510(k) number is K023618.

When did SONICAID ONE receive FDA 510(k) clearance?

SONICAID ONE received FDA 510(k) clearance on 2003-01-22, under 510(k) number K023618.

Who is the listed applicant for SONICAID ONE?

The FDA 510(k) record lists Oxford Instruments Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONICAID ONE?

The FDA product code for SONICAID ONE is HGM.

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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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